NDC 0173-0722 – Wellbutrin Sr
Bupropion Hydrochloride 200 mg/1 · Tablet, Film Coated · Oral
Product NDC0173-0722
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
- June 25, 2002
- Listing expires
- December 31, 2027
- Pharmacologic class
- Aminoketone
Active ingredients
- Bupropion Hydrochloride 200 mg/1
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 0173-0722-00 | 60 TABLET, FILM COATED in 1 BOTTLE (0173-0722-00) | Jun 25, 2002 |
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