NDC 0173-0135 – Wellbutrin Sr
Bupropion Hydrochloride 150 mg/1 · Tablet, Film Coated · Oral
Product NDC0173-0135
Product details
- Brand name
- Wellbutrin Sr
- Generic name
- bupropion hydrochloride
- Labeler
- GlaxoSmithKline LLC
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- NDA · NDA020358
- Marketed since
- November 15, 1996
- Listing expires
- December 31, 2027
- Pharmacologic class
- Aminoketone
Active ingredients
- Bupropion Hydrochloride 150 mg/1
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 0173-0135-55 | 60 TABLET, FILM COATED in 1 BOTTLE (0173-0135-55) | Nov 15, 1996 |
Other Wellbutrin products
- 0187-0730 Bupropion Hydrochloride 150 mg/1 · Tablet, Extended Release · Bausch Health US LLC
- 0187-0731 Bupropion Hydrochloride 300 mg/1 · Tablet, Extended Release · Bausch Health US LLC
- 0173-0722 Bupropion Hydrochloride 200 mg/1 · Tablet, Film Coated · GlaxoSmithKline LLC
- 0173-0947 Bupropion Hydrochloride 100 mg/1 · Tablet, Film Coated · GlaxoSmithKline LLC