NDC 63187-713 – Bupropion Hydrochloride
Bupropion Hydrochloride 150 mg/1 · Tablet, Film Coated, Extended Release · Oral
Product NDC63187-713
Product details
- Brand name
- Bupropion Hydrochloride
- Generic name
- Bupropion Hydrochloride
- Labeler
- Proficient Rx LP
- Dosage form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA077415
- Marketed since
- May 1, 2009
- Listing expires
- December 31, 2026
- Pharmacologic class
- Aminoketone
Active ingredients
- Bupropion Hydrochloride 150 mg/1
Uses, dosage, side effects and warnings for Bupropion hydrochloride →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 63187-713-30 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63187-713-30) | Jun 1, 2016 |
| 63187-713-60 | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63187-713-60) | Jun 1, 2016 |
| 63187-713-90 | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63187-713-90) | Jun 1, 2016 |
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