NDC 46708-118 – Bupropion Hydrochloride
Bupropion Hydrochloride 75 mg/1 · Tablet, Film Coated · Oral
Product NDC46708-118
Product details
- Brand name
- Bupropion Hydrochloride
- Generic name
- Bupropion Hydrochloride
- Labeler
- Alembic Pharmaceuticals Limited
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA203013
- Marketed since
- June 18, 2018
- Listing expires
- December 31, 2026
- 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 |
|---|---|---|
| 46708-118-31 | 100 TABLET, FILM COATED in 1 BOTTLE (46708-118-31) | Jun 18, 2018 |
| 46708-118-91 | 1000 TABLET, FILM COATED in 1 BOTTLE (46708-118-91) | Jun 18, 2018 |
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