NDC 0115-5445 – Bupropion Hydrochloride
Bupropion Hydrochloride 200 mg/1 · Tablet, Film Coated, Extended Release · Oral
Product NDC0115-5445
Product details
- Brand name
- Bupropion Hydrochloride
- Generic name
- Bupropion Hydrochloride
- Labeler
- Amneal Pharmaceuticals of New York LLC
- Dosage form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA076711
- Marketed since
- December 3, 2004
- Listing expires
- December 31, 2026
- Pharmacologic class
- Aminoketone
Active ingredients
- Bupropion Hydrochloride 200 mg/1
Uses, dosage, side effects and warnings for Bupropion hydrochloride →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 0115-5445-13 | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0115-5445-13) | Dec 3, 2004 |
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