NDC 72789-070 – Bupropion Hydrochloride
Bupropion Hydrochloride 100 mg/1 · Tablet, Film Coated · Oral
Product NDC72789-070
Product details
- Brand name
- Bupropion Hydrochloride
- Generic name
- Bupropion Hydrochloride
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA076143
- Marketed since
- January 17, 2006
- Listing expires
- December 31, 2027
- Pharmacologic class
- Aminoketone
Active ingredients
- Bupropion Hydrochloride 100 mg/1
Uses, dosage, side effects and warnings for Bupropion hydrochloride →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 72789-070-30 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-070-30) | Mar 26, 2020 |
| 72789-070-90 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-070-90) | Jun 7, 2024 |
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