Bupropion hcl sr 200 mg

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Author: Admin | 2025-04-28

Bupropion hydrochloride extended-release tablets (SR) for a condition for which it was not prescribed. Do not give bupropion hydrochloride extended-release tablets (SR) to other people, even if they have the same symptoms you have. They may harm them. If you take a urine drug screening test, bupropion hydrochloride extended-release tablets (SR) may make the test result positive for amphetamines. If you tell the person giving you the drug screening test that you are taking bupropion hydrochloride extended-release tablets (SR), they can do a more specific drug screening test that should not have this problem. This Medication Guide summarizes important information about bupropion hydrochloride extended-release tablets (SR). If you would like more information, talk with your healthcare provider. You can ask your healthcare provider or pharmacist for information about bupropion hydrochloride extended-release tablets (SR) that is written for healthcare professionals. For more information about bupropion hydrochloride extended-release tablets (SR), call 1- 866-495-1995. What are the ingredients in bupropion hydrochloride extended-release tablets (SR)? Active ingredient: bupropion hydrochloride USP. Inactive ingredients: colloidal silicon dioxide, diluted hydrochloride acid, hypromellose, magnesium stearate, microcrystalline cellulose, polyethylene glycol, polysorbate 80, sodium stearyl fumarate, titanium dioxide and is printed with edible black ink. In addition, the 100 mg tablet contains FD&C Red #40, the 150 mg tablet contains FD&C Blue #1 and D&C Yellow #10 Lake and the 200 mg tablet contains D&C Yellow #10 Lake. The brands listed are trademarks of their respective owners and are not trademarks of the Annora Pharma Private Limited. Medication Guide available at http://camberpharma.com/medication-guides Manufactured for: Camber Pharmaceuticals, Inc. Piscataway, NJ 08854 By: Annora Pharma Pvt. Ltd. Sangareddy - 502313, Telangana, India. This Medication Guide has been approved by the U.S. Food and Drug Administration. Revised: 05/2024 PACKAGE LABEL.PRINCIPAL DISPLAY PANEL Bupropion Tablets 100 mg 60s container Label Bupropion Tablets 150 mg 60s container Label Bupropion Tablets 200 mg 60s container Label

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