NDC 50228-144 – Bupropion Hydrochloride (XL)
Bupropion Hydrochloride 150 mg/1 · Tablet, Film Coated, Extended Release · Oral
Product NDC50228-144
Product details
- Brand name
- Bupropion Hydrochloride (XL)
- Generic name
- Bupropion hydrochloride
- Labeler
- ScieGen Pharmaceuticals,Inc.
- Dosage form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA207479
- Marketed since
- April 12, 2017
- Listing expires
- December 31, 2027
- 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 |
|---|---|---|
| 50228-144-05 | 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (50228-144-05) | Apr 12, 2017 |
| 50228-144-30 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (50228-144-30) | Apr 12, 2017 |
| 50228-144-90 | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (50228-144-90) | Apr 12, 2017 |
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