NDC 63187-052 – Bupropion hydrochloride
Bupropion Hydrochloride 150 mg/1 · Tablet, Film Coated, Extended Release · Oral
Product NDC63187-052
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 · ANDA078866
- Marketed since
- April 8, 2010
- 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 |
|---|---|---|
| 63187-052-30 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63187-052-30) | May 1, 2014 |
| 63187-052-60 | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63187-052-60) | May 1, 2014 |
| 63187-052-78 | 180 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63187-052-78) | May 1, 2014 |
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