No. 3861 — Tablets ZETIA, 10 mg, are white to off-white, capsule-shaped tablets debossed with "414" on one side. They are supplied as follows: NDC 66582-414-31 bottles of 30 NDC 66582-414-54 bottles of 90 NDC 66582-414-74 bottles of 500 NDC 66582-414-76 bottles of 5000 NDC 66582-414-28 unit dose packages of 100.
Actived: 3 days ago
The National Library of Medicine (NLM)’s DailyMed searchable database provides the most recent labeling submitted to the Food and Drug Administration (FDA) by companies and currently in use (i.e., "in use" labeling). DailyMed contains labeling for prescription and nonprescription drugs for human and animal use, and for additional products such as medical gases, devices, cosmetics, dietary
Bupropion Hydrochloride Extended-release Tablets USP (XL), 300 mg of bupropion hydrochloride, are off-white to pale yellow, round, biconvex, coated tablets imprinted with "L016" in black ink on one side and plain on the other side. Seizure disorder. (4,5.3) Current or prior diagnosis of bulimia or anorexia nervosa (4, 5.3) Abrupt
Mirtazapine tablets, USP 7.5 mg, 15 mg, 30 mg and 45 mg
45 mg tablets-White to off-white colored, oval, biconvex, film coated tablets with "501" debossed on one side and plain on the other side. Storage Store at 20° to 25°C (68° to 77°F); excursions permitted 15° to 30°C (59° to 86°F). [see USP Controlled Room Temperature]. Protect from light and moisture.
Albuterol sulfate is a white to off-white crystalline powder. It is soluble in water and slightly soluble in ethanol. Albuterol sulfate is the official generic name in the United States, and salbutamol sulfate is the World Health Organization recommended generic name. Albuterol Sulfate HFA Inhalation Aerosol is a pressurized metered-dose
Ciclopirox Shampoo, 1%
Ciclopirox Shampoo 1% contains the synthetic antifungal agent, ciclopirox. Each gram (equivalent to 0.96 mL) of Ciclopirox Shampoo contains 10 mg ciclopirox in a shampoo base consisting of disodium laureth sulfosuccinate, laureth-2, purified water USP, sodium chloride USP and sodium laureth sulfate. Ciclopirox Shampoo is a colorless to
Consider contacting a poison control center (1-800-222-1222 or www.poison.org) for additional information on the treatment of overdosage. Close. 11 DESCRIPTION. CYMBALTA® (duloxetine delayed-release capsules) is a selective serotonin and norepinephrine reuptake inhibitor (SNRI) for …
Fioricet 50 mg/300 mg/40 mg. Containing 50 mg butalbital, 300 mg acetaminophen, and 40 mg caffeine. Available as hard gelatin capsules with a light blue opaque body and a light blue opaque cap. Cap is imprinted twice with "FIORICET" in black and body is imprinted twice with a three-head profile " " in black.
Pantoprazole Sodium DR 40 MG
Pantoprazole sodium sesquihydrate is a white to off-white crystalline powder and is racemic. Pantoprazole has weakly basic and acidic properties. Pantoprazole sodium sesquihydrate is freely soluble in water, very slightly soluble in phosphate buffer at pH 7.4, and practically insoluble in n-hexane.
PRESCRIBING INFORMATION ZOVIRAX® (acyclovir) Ointment 5%
ZOVIRAX Ointment 5% is a formulation for topical administration. Each gram of ZOVIRAX Ointment 5% contains 50 mg of acyclovir in a polyethylene glycol (PEG) base. Acyclovir is a white to off-white crystalline powder with the molecular formula C 8 H 11 N 5 O 3 and a molecular weight of 225.20. The maximum solubility in water at 37°C is 2.5 mg/mL.
Transderm Scōp (scopolamine transdermal system) 1 mg/3 days is available as the following: Carton of 4 transdermal systems, packaged into individual foil pouches. NDC 0067-4346-04. Store at controlled room temperature between 68°F to 77°F (20°C to 25°C). Store pouch (es) in an upright position.
Dorzolamide hydrochloride has a molecular weight of 360.91. It is a white to off-white, crystalline powder, which is soluble in water and slightly soluble in methanol and ethanol. Timolol maleate is described chemically as: (-)-1-(tert-butylamino)-3-[(4-morpholino-1,2,5-thiadiazol-3-yl)oxy]-2-propanol maleate (1:1) (salt). Timolol maleate
If the patch falls off before 72 hours, dispose of it by folding in half and flushing down the toilet. A new patch may be applied to a different skin site. Patients (or caregivers who apply fentanyl transdermal system) should wash their hands immediately with soap and water after applying fentanyl transdermal system.
Ammonium Lactate Cream, 12%*
DESCRIPTION. *Ammonium Lactate Cream, 12% is a formulation of 12% lactic acid neutralized with ammonium hydroxide, as ammonium lactate with a pH of 4.4 - 5.4. Ammonium Lactate Cream, 12% also contains cetyl alcohol, glycerin, glyceryl stearate, laureth-4, light mineral oil, magnesium aluminum silicate, methylcellulose, methylparaben, PEG-100
NICOTINE TRANSDERMAL SYSTEM, STEP 1, STEP 2, STEP 3
Step 1. Step 2. Step 3. Use one 21 mg patch/day. Use one 14 mg patch/day. Use one 7 mg patch/day. if you smoke 10 or less cigarettes per day, start with Step 2 for 6 weeks, then Step 3 for 2 weeks. apply one new patch every 24 hours on skin that is dry, clean and hairless. remove backing from patch and immediately press onto skin.
FORTAZ® (ceftazidime for injection)
FORTAZ ® is a dry, white to off-white powder supplied in vials as follows: NDC 52565-105-10 500-mg* Single-Dose Vial (Carton of 10) NDC 52565-106-10 1-g* Single-Dose Vial (Carton of 10) NDC 52565-107-10 2-g* Single-Dose Vial (Carton of 10) * Equivalent to anhydrous ceftazidime.
Naloxone Hydrochloride 1mg/1ml 2ml Syringe
DESCRIPTION. Naloxone hydrochloride, a narcotic antagonist, is a synthetic congener of oxymorphone. In structure it differs from oxymorphone in that the methyl group on the nitrogen atom is replaced by an allyl group. 17-Allyl-4,5a-epoxy-3,14-dihydroxymorphinan-6-one hydrochloride C19H21NO4• HCl 363.84 Naloxone hydrochloride occurs as a white to slightly off-white powder, and is soluble in
Albuterol Sulfate Inhalation Solution, 0.083% 2.5 mg*/3 ml
Albuterol sulfate inhalation solution 0.083% requires no dilution before administration. Each mL of albuterol sulfate inhalation solution (0.083%) contains 0.83 mg of albuterol (as 1 mg of albuterol sulfate) in an isotonic, sterile, aqueous solution containing sodium chloride; sulfuric acid is used to adjust the pH to between 3 and 5.
OMNIPAQUE™ (iohexol) Injection 300 350
Movement onto and off the stretcher should be done slowly with the patient completely passive, maintaining head-up position. Before moving patient onto bed, raise head of bed 30° to 45°. Advise patient to remain still in bed, in a sitting or semisitting position, especially in the first few hours.
Graxcell Pharmaceutical Sodium Chloride Tablets, USP
Directions. to make isontonic solution of sodium chloride, dissolve one tablet in 120 ml (four ounces) of distilled water and use as directed by a physician. if used as an electrolyte replenisher for the prevention of heat cramps due to excessive perspiration take one tablet orally as. directed by your physician.
If skin dryness occurs, it may be controlled by rinsing off sooner or using less frequently. HOW SUPPLIED Sodium Sulfacetamide 9.8% - Sulfur 4.8% Cleanser is supplied in a 10 oz (285 g) bottle (NDC 42192-156-10). STORAGE. Store at 20º to 25ºC (68º to 77ºF), excursions permitted between 15º and 30ºC (between 59º and 86ºF). [See USP
Topicort® (Desoximetasone Cream USP) 0.05%
DESCRIPTION. Topicort ® (desoximetasone cream USP) 0.05%, Topicort ® (desoximetasone cream USP) 0.25%, and Topicort ® (desoximetasone gel USP) 0.05% contain the active synthetic corticosteroid desoximetasone. The topical corticosteroids constitute a class of primarily synthetic steroids used as anti-inflammatory and antipruritic agents.
Clonidine Transdermal System(clonidine)
System Structure and Components: Clonidine Transdermal System is a multi-laminate patch, 0.3 mm thick, containing clonidine as the active agent. The patch surface areas are 10.8 cm 2 (Clonidine Transdermal System 0.1 mg/day), 21.6 cm 2 (Clonidine Transdermal System 0.2 mg/day), and 32.4 cm 2 (Clonidine Transdermal System 0.3 mg/day). The composition per unit area is the same for all three …
Dr.Reddys Laboratories Inc BUPRENORPHINE AND …
patient off of the opioid. (5.6) Risk of Opioid Withdrawal with Abrupt Discontinuation: If treatment is temporarily interrupted or discontinued, monitor patients for withdrawal and treat appropriately. (5.7) Risk of Hepatitis, Hepatic Events: Monitor liver function tests prior to initiation and during treatment and evaluate suspected hepatic
Alprazolam, USP is a white to off-white crystalline powder, which is soluble in methanol or ethanol but which has no appreciable solubility in water at physiological pH. Each tablet, for oral administration, contains 0.25 mg, 0.5 mg, 1 mg, or 2 mg of alprazolam, USP. The 2 mg tablets are multi-scored and may be divided in half to provide two 1
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Gently pull off the outer needle shield and put it on a flat surface. You will use the outer needle shield later to remove the needle from the Pen after the injection is finished. See Figure I. Figure I. Note: Check that the cartridge holder is attached to the Pen body before each injection. One of the blue arrows on the cartridge should be
Desvenlafaxine succinate is a white to off-white powder that is soluble in water. The solubility of desvenlafaxine succinate is not pH dependent. The solubility in water is about 50 mg per mL. Desvenlafaxine is formulated as an extended-release tablet for once-a-day oral administration containing 38 mg, 76 mg or 152 mg of desvenlafaxine
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Warning: Do not flip the blue safety release off using a thumb or by pulling it sideways, or by bending and twisting the blue safety release. This may cause the real yellow EpiPen or real green EpiPen Jr auto-injector to accidentally activate. An EpiPen or EpiPen Jr auto-injector that has been activated by accident cannot be used for a patient
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2. Pull Red safety guard down and off of AUVI-Q. See Figure C. To reduce the chance of an accidental injection, do not touch the black base of the auto-injector, which is where the needle comes out. If an accidental injection happens, get medical help right away. Note: The red safety guard is made to fit tight. Pull firmly to remove. Figure C. 3.
Apply patch on intact skin for a 24-hour period; replace with a new patch every 24 hours. (2.1, 2.4) Initial Dose: Initiate treatment with 4.6 mg/24 hours Rivastigmine Patch Dose Titration (2.1): After a minimum of 4 weeks, if tolerated, increase dose to 9.5 mg/24 hours, which is the minimum effective dose . Following a minimum additional 4 weeks, may increase dosage to maximum dosage of 13.3
Its molecular formula is C 15 H 19 N 5 •C 7 H 6 O 2, representing a molecular weight of the free base of 391.47 g/mol. Rizatriptan benzoate is a white to off-white powder that is soluble in methanol; sparingly soluble in water; slightly soluble in acetone and ethanol.
Sandoz Inc ESTRADIOL TRANSDERMAL SYSTEM- estradiol patch
In the event that a system should fall off reapply it to a different location. If the system cannot be reapplied, a new system should be applied for the remainder of the 7-day dosing interval. Only one system should be worn at any one time during the 7-day dosing interval.
Lannett Company, Inc. PANTOPRAZOLE SODIUM- …
40 mg, white to off-white, oval-shaped coated tablet, debossed with “17” on one side 20 mg, white to off-white, oval-shaped coated tablet, imprinted in black with “18” on one side 4 CONTRAINDICATIONS Pantoprazole is contraindicated in patients with known hypersensitivity to any component of the formulation or any substituted benzimidazole.
If a system should fall off, the same system may be reapplied to another area of the lower abdomen. If necessary, a new transdermal system may be applied, in which case, the original treatment schedule should be continued. Only 1 system should be worn at any 1 time during the 3- to 4-day dosing interval. Once in place, the transdermal system
Myfortic, as the sodium salt, is a white to off-white, crystalline powder and is highly soluble in aqueous media at physiological pH and practically insoluble in 0.1N hydrochloric acid. Myfortic is available for oral use as delayed-release tablets containing either 180 mg or 360 mg of mycophenolic acid.
Budesonide is a white to off-white, tasteless, odorless powder which is practically insoluble in water and in heptane, sparingly soluble in ethanol, and freely soluble in chloroform. Its partition coefficient between octanol and water at pH 7.4 is 1.6 x 10 3.
Teva Pharmaceuticals USA, Inc. ESTRADIOL- estradiol insert
Estradiol vaginal inserts USP are white to off-white, round, film-coated, unscored, biconvex inserts containing 10 mcg of estradiol. Each vaginal insert is 6 mm in diameter and is administered in a disposable applicator. 4 CONTRAINDICATIONS Estradiol vaginal inserts should not be used in women with any of the following conditions: