NDC 50090-6871 – Bupropion Hydrochloride SR
Bupropion Hydrochloride 150 mg/1 · Tablet, Film Coated, Extended Release · Oral
Product NDC50090-6871
Product details
- Brand name
- Bupropion Hydrochloride SR
- Generic name
- bupropion hydrochloride
- Labeler
- A-S Medication Solutions
- 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 (4)
| Package NDC | Description | Since |
|---|---|---|
| 50090-6871-0 | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-6871-0) | Dec 4, 2023 |
| 50090-6871-1 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-6871-1) | Dec 4, 2023 |
| 50090-6871-2 | 180 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-6871-2) | Dec 4, 2023 |
| 50090-6871-3 | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-6871-3) | Dec 4, 2023 |
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