What is the generic name 83396726NDC 50419-754-01CIPRO®(ciprofloxacin hydrochloride)Equivalent to500mg ciprofloxacin100TabletsR OnlyAttentlon Pharmacist:Dispense the enclosedMedication Gulde to each patient.Manufactured byBayer HealthCare Pharmaceuticalo Inc.Wayne, NJ 07470Made in Gemanyhat.the seneric name?Printed In USA6505-01-333-41540011Bayer HealthCare Phamaceuticals Inc.15783)CIPRO S a regstered trademark of Bayer Aktiengesellschaft.DESCRIPTION: Each tablet contains ciprofloxacinhydrochloride equivalent to 500 mg of ciprofloxacin.DOSAGE: See accompanying literature for completeInformation on dosage and administration.RECOMMENDED STORAGE:Store below 86°F (30°C).Batch:Expires:

Antibiotics are defined as the type of medications where they are used for treating infections or…

Answered: 83396726 NDC 50419-754-01 CIPRO®…

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83396726 NDC 50419-754-01 CIPRO® (ciprofloxacin hydrochloride) Equivalent to

Curren'S Math For Meds: Dosages & Sol

11th Edition

ISBN:9781305143531

Author:CURREN

Publisher:CURREN

Chapter6: Oral Medication Labels And Dosage Calculation

Section: Chapter Questions

Problem 6.1P

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use the label below for this question order; valproic acid o•075 Po Tio) per dose, give :
Generic name Brand name Manufacturer National Drug Code (N D C) # Lot number (control number) Drug form Dosage strength Usual adult dose Total amount in vial, packet, box Prescription warning Expiration date NDC 68083-320-01 Rx only Dicyclomine Hydrochloride Injection, USP 20 mg/2 mL (10 mg/mL) For Intramuscular Use Only 2 mL Single-Dose Vial Store at 20° to 25°C (68° to 77°F) (See Insert). Protect from freezing. Discard unused portion. APC Pharmaceuticals, LLC 7101 Falling Springs Road, Manufactured for: Fort Worth Texas 76116 USA Made in India. M.L. No.: 103/AP/RR/97/F/R LAB-XXXXXX-XX (01) 00368063 32001 6 18 x 10 mm Unvarnish area Lot: Exp.:
NOC 16571-013-01 Piroxicam Capsules USP, 20 mg Rev. 00 PHARMACIST: Dispense the enclosed Medication Guide to each patient 100 Capsules R Only PACK PHARMACEVTICALA LIC USUAL DOSAGE: See Package Insert. Store at 20-25°C (68-77°F): excursions permitted to 15-30°C (59-86°F). [See USP Controlled Room Temperature.] WARNING: AS WITH ALL MEDICATIONS, KEEP OUT OF REACH OF CHILDREN. EACH CAPSULE CONTAINS: Piroxicam USP 20 mg Dispense in a tight, light-resistant container as defined in the USP Manufactured by Nostrum Laboratories, Inc. Kansas City, MO 64120 Distributed by: PACK Pharmaceuticals, LLC Buffalo Grove, IL 60089 16571 01301 2 Non Varnish Area Lot No: Exp. Date: Use the medication label to complete these calculations. The drug label will supply the dosage strength and the unit. The healthcare provider orders 80 mg of piroxicam per day. How many capsules should be given for this dose?
Doctors order Tazicef (ceftazidime) 1.5 g IV Q12H. Refer to the label below. How much Tazicef will you draw up for one dose? NDC 0409-5086-11 equivalent to 6 grams ceftazidime TAZICEF® Store at 20° to 25°C (68' to 7) (See USP Controled Room Temperaturel Primarily for institutional use. MPÓRTANT: This vial is under reduced pressure, Addition of diluent generates a positive pressure. Before reconstituting, see Instructions for Reconstitution. Usual Adult Dosage: 1 gram every 8 to 12 hours. Ih severe, refractory or Ite-threatening infections, 2 grams every 8 hours. See accompanying prescribing information. In two stages, add Sodium Chloride Injection, Sterile Water for Injection or Bacteriostatic Water for Injection according to table below. See accompanying prescribing information. SHAKE WELL, Use promptly. (Discard vial within 4 hours after initial entry.) Ceftazidime For Injection, USP Approx. Concentration Amount of Duent gram/5 ml 1 gram/10 mL 26 mL 56 mL 10 PHARMACY BULK VIALS NOT…
Generic name Brand name Manufacturer National Drug Code (N D C) # Lot number (control number) Drug form Dosage strength Usual adult dose Total amount in vial, packet, box Prescription warning Expiration date AUGMENTIN® Tear along perforation NSN 6505-01-340-0847 Directions for mixing: Tap bottle until all powder flows freely. Add approximately 2/3 of total water for reconstitution (total = 67 mL): shake vigorously to wet powder. Add remaining water, again shake vigorously. Dosage: See accompanying prescribing information. Tear along perforation Keep tightly closed. Shake well before using. Must be refrigerated. Discard after 10 days. 125mg/5mL NDC 0029-6085-39 AUGMENTIN® AMOXICILLIN/ CLAVULANATE POTASSIUM FOR ORAL SUSPENSION When reconstituted, each 5 mL contains: AMOXICILLIN, 125 MG, as the trihydrate CLAVULANIC ACID, 31.25 MG, as clavulanate potassium 75mL (when reconstituted) SB SmithKline Beecham
Generic name Brand name Manufacturer National Drug Code (N D C) # Lot number (control number) Drug form Dosage strength Usual adult dose Total amount in vial, packet, box Prescription warning Expiration date Contains 1 mg edetate disodium Store at 20°-25°C (68-77°F); excursions permitted to 15-30°C (59-86°F). [See USP Controlled Room Temperature]. Protect vials from light; use of vial carton is recommended. Distributed by Wyeth Pharmaceuticals Inc A subsidiary of Pfizer Inc Philadelphia, PA 19101 Under license from Takeda GmbH D78467 Konstanz, Germany MADE IN FRANCE 14278100 F.1/0813/ 6083672 6 0008-0923-55 1 Bundle of 10 unit cartons NDC 0006-0023-55 PROTONIX® I.V. (pantoprazole sodium) for Injection Equivalent to 40 mg pantoprazole per vial For L.V. infusion only. Pfizer Injectables LOT Rx only EXP ‒‒‒‒
NDC 63323-359-03 305903 KANAMYCIN INJECTION, USP *1 g/3 mL (333 mg/mL) For IM or IV Use 3 mL Vial 10 Vials Rx only Using the label above, how many mL of Kanamycin must be administered to a patient in which the orders read 275 mg IM stat. Give your answer to 2 decimal places. Type mL in the units box. Your Answer: Answer units quas *Each ml. contains lanamycin sulfate equivalent to 333 mg kan amycin. 0.45% sodium bisulfite added as an antioxidant, buffered with sodium citrate (2.2 %). Adjusted to pH 4.5 with H,S0 Kanamycin Injection should not be physically mixed with other antibaderial agents Usual Dosage: Intramuscular 7.5 mg/kg of body weight at 12-hour intervals. Do not exceed 1.5grams daily. See insert for IV and other uses Vial stoppers do not contain natural rubber latex. Store at 20° to 25°C (68 to 77 F) [see USP Cantrdled Room Temperature]. Avoid freezing. APP APP Pharmaceuticals, LLC Schaumburg, IL 60173 63323-359-03 42650D LOT/EXP
Acetaminophen (Drug Monograph) In the identification test using infrared absorption, name the reagent where the specimen should be suspended.
A patient is prescribed venlafaxine 37.5 mg daily for 7 days, increasing by 37.5 mg every week until a maximum daily dose of 225 mg is reached. A total of 8 weeks treatment must be dispensed. You supply your total stock of 84 venlafaxine 37.5 mg tablets. How many tablets are still owed to the patient?
ONDANSETRON NDC 55390-121-10 INJECTION USP 2 mL Single Dose Vial Rx ONLY 4 mg/2 mL 2 mg/mL Mfg for: Bedford Labs Bedford, OH 44146 OND-V01 Use the medication label to complete these calculations. The drug label will supply the dosage strength and the unit. The nurse is working in the recovery room and has ondansetron 3 mg ordered for a patient. The nurse would give milliliters (mL) of the medication per dose?
Ordered: Cefadroxil 0.6 g PO q8h for a patient with cystitis. NDC 68180-181-02 Usual Dosage: See package insert for complete dosage information. Cefadroxil for Oral Directions for Reconstitution: Tap bot de lightly to loosen powder. Add 67 mL of water in two portions. Shake well after each addition. Suspension USP 250 mg/5 mL When mixed as directed, each 5 mL (approximately one teaspoonful) will contain cefadroxil monohydrate USP equivalent to 250 mp cetadroxil. Rx only LUPIN 100 mL when mixed 1 What is the form of the medication? Oral Prior to Reconstitution: Store at 25°C (77°F); excursions permitted to 15-30 C (59-86°F). [See USP Controlled Room Temperature). SHAKE WELL BEFORE USING. After Reconstitution: Store in refrigerato Keep container tightly closed. Discard unused portion after 14 days. Manufactured for Lupin Pharmaceuticals, Inc. Baltimore, Maryland 21202 United States Manufactured by Lupin Limited Mumbai 400 098 INDIA Code No. MP DRUGS/28/18.88 What is the type of diluent…
Order Meperidine (Demerol) 50mg IV q4h prn. Refer to the label below. How much will you draw up to administer per dose? Nop-Catel srg e re, NOC 0641-054-25 Ronly Meperidine HCI Injection, USP Ench ml contains meperidine hydracho ride 100 mg in Water for Injection Buered with acetic acisedum otate Ual L Do not ine If preoptated Store at e ( rn (See USP Controlled Reem Temperature). e See package |100 mg/mL (0 25 x1 ml Single Dose Vials FOR INTRAMUSCULAR, SUBCUTANEOUS OR SLOW INTRAVENOUS USE WWETWARD