NDC 59651-848 – Bupropion Hydrochloride
Bupropion Hydrochloride 200 mg/1 · Tablet, Film Coated, Extended Release · Oral
Product NDC59651-848
Product details
- Brand name
- Bupropion Hydrochloride
- Generic name
- Bupropion Hydrochloride
- Labeler
- Aurobindo Pharma Limited
- Dosage form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA090325
- Marketed since
- June 3, 2025
- 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 (2)
| Package NDC | Description | Since |
|---|---|---|
| 59651-848-01 | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (59651-848-01) | Jun 3, 2025 |
| 59651-848-60 | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (59651-848-60) | Jun 3, 2025 |
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