NDC 72189-057 – Bupropion Hydrochloride
Bupropion Hydrochloride 100 mg/1 · Tablet, Extended Release · Oral
Product NDC72189-057
Product details
- Brand name
- Bupropion Hydrochloride
- Generic name
- Bupropion Hydrochloride
- Labeler
- DIRECT RX
- Dosage form
- Tablet, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA202304
- Marketed since
- November 8, 2019
- Listing expires
- December 31, 2026
- Pharmacologic class
- Aminoketone
Active ingredients
- Bupropion Hydrochloride 100 mg/1
Uses, dosage, side effects and warnings for Bupropion hydrochloride →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 72189-057-30 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-057-30) | Nov 8, 2019 |
| 72189-057-60 | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-057-60) | Nov 8, 2019 |
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