NDC 50090-4049 – Bupropion Hydrochloride XL
Bupropion Hydrochloride 150 mg/1 · Tablet, Film Coated, Extended Release · Oral
Product NDC50090-4049
Product details
- Brand name
- Bupropion Hydrochloride XL
- Generic name
- Bupropion Hydrochloride
- Labeler
- A-S Medication Solutions
- Dosage form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA077715
- Marketed since
- November 26, 2008
- 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 (3)
| Package NDC | Description | Since |
|---|---|---|
| 50090-4049-0 | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-4049-0) | Jan 11, 2019 |
| 50090-4049-1 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-4049-1) | Jan 11, 2019 |
| 50090-4049-2 | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-4049-2) | Jan 11, 2019 |
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