NDC 43547-289 – bupropion hydrochloride SR
Bupropion Hydrochloride 150 mg/1 · Tablet, Film Coated, Extended Release · Oral
Product NDC43547-289
Product details
- Brand name
- bupropion hydrochloride SR
- Generic name
- bupropion hydrochloride
- Labeler
- Solco Healthcare US LLC
- Dosage form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA202304
- Marketed since
- November 1, 2014
- 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 (5)
| Package NDC | Description | Since |
|---|---|---|
| 43547-289-06 | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (43547-289-06) | Nov 1, 2014 |
| 43547-289-09 | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (43547-289-09) | Nov 1, 2014 |
| 43547-289-10 | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (43547-289-10) | Nov 1, 2014 |
| 43547-289-25 | 250 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (43547-289-25) | Nov 1, 2014 |
| 43547-289-50 | 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (43547-289-50) | Nov 1, 2014 |
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