NDC 0187-0730 – Wellbutrin Xl
Bupropion Hydrochloride 150 mg/1 · Tablet, Extended Release · Oral
Product NDC0187-0730
Product details
- Brand name
- Wellbutrin Xl
- Generic name
- Bupropion hydrochloride
- Labeler
- Bausch Health US LLC
- Dosage form
- Tablet, Extended Release
- Route
- Oral
- Marketing category
- NDA · NDA021515
- Marketed since
- August 29, 2003
- Listing expires
- December 31, 2027
- Pharmacologic class
- Aminoketone
Active ingredients
- Bupropion Hydrochloride 150 mg/1
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 0187-0730-07 | 7 TABLET, EXTENDED RELEASE in 1 BOTTLE (0187-0730-07) | Aug 29, 2003 |
| 0187-0730-30 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (0187-0730-30) | Aug 29, 2003 |
| 0187-0730-90 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (0187-0730-90) | Aug 29, 2003 |
Other Wellbutrin products
- 0187-0731 Bupropion Hydrochloride 300 mg/1 · Tablet, Extended Release · Bausch Health US LLC
- 0173-0135 Bupropion Hydrochloride 150 mg/1 · Tablet, Film Coated · GlaxoSmithKline 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