NDC 59651-512 – Bupropion Hydrochloride
Bupropion Hydrochloride 300 mg/1 · Tablet, Film Coated, Extended Release · Oral
Product NDC59651-512
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 · ANDA216051
- Marketed since
- July 21, 2026
- Listing expires
- December 31, 2027
- Pharmacologic class
- Aminoketone
Active ingredients
- Bupropion Hydrochloride 300 mg/1
Uses, dosage, side effects and warnings for Bupropion hydrochloride →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 59651-512-05 | 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (59651-512-05) | Jul 21, 2026 |
| 59651-512-30 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (59651-512-30) | Jul 21, 2026 |
| 59651-512-90 | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (59651-512-90) | Jul 21, 2026 |
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