NDC 43063-880 – Bupropion Hydrochloride
Bupropion Hydrochloride 75 mg/1 · Tablet, Film Coated · Oral
Product NDC43063-880
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 75 mg/1
Uses, dosage, side effects and warnings for Bupropion hydrochloride →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 43063-880-30 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-880-30) | Aug 13, 2018 |
| 43063-880-60 | 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-880-60) | Oct 30, 2018 |
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