NDC 71209-052 – Bupropion Hydrochloride
Bupropion Hydrochloride 75 mg/1 · Tablet, Film Coated · Oral
Product NDC71209-052
Product details
- Brand name
- Bupropion Hydrochloride
- Generic name
- Bupropion Hydrochloride
- Labeler
- Cadila Pharmaceuticals Limited
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA208606
- Marketed since
- January 16, 2020
- 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 (3)
| Package NDC | Description | Since |
|---|---|---|
| 71209-052-05 | 100 TABLET, FILM COATED in 1 BOTTLE (71209-052-05) | Jan 12, 2023 |
| 71209-052-11 | 1000 TABLET, FILM COATED in 1 BOTTLE (71209-052-11) | Jan 12, 2023 |
| 71209-052-17 | 10 BLISTER PACK in 1 CARTON (71209-052-17) / 10 TABLET, FILM COATED in 1 BLISTER PACK | Jan 12, 2023 |
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