Bupropion Hydrochloride Sr 71335-0135
Generic: Bupropion Hydrochloride
Product NDC
71335-0135- Manufacturer
- Bryant Ranch Prepack
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- July 2, 2009
- Listing Expires
- December 31, 2026
- Application
- ANDA079095
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Bupropion Hydrochloride | 150 mg/1 |
Drug Class
Packaging Options(9)
60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0135-1)
90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0135-2)
30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0135-3)
120 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0135-4)
45 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0135-5)
180 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0135-6)
28 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0135-7)
56 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0135-8)
100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0135-9)