Label 1 Each Extended Release Tablet Contains Bupropion Hydrochloride Usp 100 Mg Usual Dosage See Accompanying Lite 1 (53.33 KiB) Viewed 10 times
Label 1 Each Extended Release Tablet Contains Bupropion Hydrochloride Usp 100 Mg Usual Dosage See Accompanying Lite 2 (17.46 KiB) Viewed 10 times
Label 1 Each Extended Release Tablet Contains Bupropion Hydrochloride Usp 100 Mg Usual Dosage See Accompanying Lite 3 (15.8 KiB) Viewed 10 times
Label #1 Each extended-release tablet contains: Bupropion Hydrochloride, USP 100 mg. Usual Dosage: See accompanying literature for complete prescribing and dosage information Store at 20° to 25°C (68° to 77°F) (see USP Controlled Room Temperature). Dispense contents in a tight, light-resistant container as defined in the USP with a child-resistant closure, as required. Protect from light and moisture. Keep tightly closed. KEEP OUT OF THE REACH OF CHILDREN. ZYBAN is a registered trademark of GlaxoSmithKline Manufactured for Sander Inc., Princeton, NJ 085-40 Manufactured by Epic Pharma, LLC, Laurelton, NY 11413 Product of Italy R10/2017 L6082 Label #2 37250800415 291000000 1015 Reading the Label Directions for mixing: 1. Tap bottle to loosen ALL powder 2. Measure a total of 130 m OF WATER 3. Add approximately 20 (about 87 m.) of the water to the powder Replace cap and VIGOROUSLY. 4. Add remaining water (about 43 m) Replace cap and shake VIGOROUSLY Desage: See accompanying prescribing information Keep tightly closed. Shake well before each use. Store reconstituted suspension in refrigerator. Discard after 10 days. Some color change is normal during dosing period. NDC 0185-0410-60 BUPROPion Hydrochloride Extended-Release Tablets, USP (SR) Twice-A-Day 100 m 0 mg ti WARNING: Do not use in combination with ZYBAN or any other medicines that contain hapropion hydrochloride PHARMACIST: Dispense with attached Medication Guide Rx Only 60 Tablets SANDOZ AUGMENTIN® AMOXICILLIN/ CLAVULANATE POTASSIUM FOR ORAL SUSPENSION When reconstituted, each 5 mL contains: AMOXICILLIN, 250 MG. as the trihydrate CLAVULANIC ACID, 62.5 MG, as clavulanate potassium 150 mL (when reconstituted) neopharma Rx only 11218 Rapp 150060821 Use only if inner seal is intact. Net Cry Md. By: Neopharma Tennessee LLC, Bristol, TN 37620 Store dry powder at or below 25° C (77° F). 0185-0410-60
Label #1 1. Trade name 2. Generic name 3. Total volume or amount 4. Form 5. Route 6. Dosage strength Reading the Label 7. Controlled substance schedule 8. Storage information 9. Manufacturer's name 10. Does it have a black box warning?
Label 2 11. Trade name 12. Generic name 13. Total volume or amount 14. Form 15. Route 16. Dosage strength 17. Controlled substance schedule 18. Storage information 19. Manufacturer's name 20. Does it have a black box warning?
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