8. ch m NDC 62037-571-01 Metformin Hydrochloride Extended-Release Tablets, USP M Actavis 10. NDC 0703 8416-01 9. NOC 014

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8. ch m NDC 62037-571-01 Metformin Hydrochloride Extended-Release Tablets, USP M Actavis 10. NDC 0703 8416-01 9. NOC 014

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8 Ch M Ndc 62037 571 01 Metformin Hydrochloride Extended Release Tablets Usp M Actavis 10 Ndc 0703 8416 01 9 Noc 014 1
8 Ch M Ndc 62037 571 01 Metformin Hydrochloride Extended Release Tablets Usp M Actavis 10 Ndc 0703 8416 01 9 Noc 014 1 (55.76 KiB) Viewed 32 times
8. ch m NDC 62037-571-01 Metformin Hydrochloride Extended-Release Tablets, USP M Actavis 10. NDC 0703 8416-01 9. NOC 0143-1241-41 Digoxin Tablets, USP 250 mcg (0.25 mg) 100 TABLETS 1 Only WESTWARD Each Extended Release Tablet Contains Metformin Hydrochloride USP 500 mg Dispense in a light-resistant container Usual Dosage See enclosed package age information to 25°C 168 to 771 [See USP Controlled Room Temperature 22571 Manufactured by Watson Phamma Private Limited 100 Tablets Rx Only Verna, Salcette Goa 403 722 INDIA Distributed by Actavis Pharmia, Inc. Parsippany, NJ 07054 USA 02/16 Rs only Each ml contains tabramycin sulfate equivalent to 40 mg tobramycin, phenol 5 mg; sodium metabisulfite 3.2 mg, edetate disodium 0.1 mg, water for injection qs: pH is adjusted with sulfuric acid and if necessary sedium hydroxide. pH 3.0 106.5. Usual Desage: See Package Insert Store at 20 to 25°C (68 to 17"F). (See USP Controlled Room Temperaturel. SAMPLE TEVA PHARMACEUTICALS USA, INC. North Wales, PA 19454 Rev. A 6/2015 Tobramycin Injection USP 40 mg/mL 30 mL Multiple Dose Vial For IM or IV Dilute Before IV Use TEMA 500 mg SAMPLE SAMINE SEOTTA CHAPTER 2 The Drug Label 3 a. The label indicates that 250 mcg YES/NO is equivalent to 0.25 mg. b. This drug label identifies a boxed warning. YES/NO a. The dosage strength is 571 mg per YES/NO tablet. YES/NO b. The tablet may be chewed or crushed. a. The total amount in the vial is 30 mL. b. The routes of administration include IM or IV. YES/NO YES/NO
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