NDC 63187-819 – Bupropion Hydrochloride
Bupropion Hydrochloride 300 mg/1 · Tablet, Extended Release · Oral
Product NDC63187-819
Product details
- Brand name
- Bupropion Hydrochloride
- Generic name
- Bupropion Hydrochloride
- Labeler
- Proficient Rx LP
- Dosage form
- Tablet, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA077285
- Marketed since
- February 17, 2015
- Listing expires
- December 31, 2026
- Pharmacologic class
- Aminoketone
Active ingredients
- Bupropion Hydrochloride 300 mg/1
Uses, dosage, side effects and warnings for Bupropion hydrochloride →
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 63187-819-30 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (63187-819-30) | Feb 1, 2017 |
| 63187-819-60 | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (63187-819-60) | Feb 1, 2017 |
| 63187-819-78 | 180 TABLET, EXTENDED RELEASE in 1 BOTTLE (63187-819-78) | Feb 1, 2017 |
| 63187-819-90 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (63187-819-90) | Feb 1, 2017 |
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