NDC 68071-2890 – Bupropion Hydrochloride SR
Bupropion Hydrochloride 150 mg/1 · Tablet, Film Coated, Extended Release · Oral
Product NDC68071-2890
Product details
- Brand name
- Bupropion Hydrochloride SR
- Generic name
- Bupropion hydrochloride
- Labeler
- NuCare Pharmaceuticals,Inc.
- Dosage form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA205794
- Marketed since
- April 20, 2018
- Listing expires
- December 31, 2026
- Pharmacologic class
- Aminoketone
Active ingredients
- Bupropion Hydrochloride 150 mg/1
Uses, dosage, side effects and warnings for Bupropion hydrochloride →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 68071-2890-3 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (68071-2890-3) | Nov 30, 2022 |
| 68071-2890-6 | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (68071-2890-6) | Aug 26, 2025 |
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