NDC 50090-4747 – Bupropion Hydrochloride
Bupropion Hydrochloride 150 mg/1 · Tablet, Extended Release · Oral
Product NDC50090-4747
Product details
- Brand name
- Bupropion Hydrochloride
- Generic name
- Bupropion Hydrochloride
- Labeler
- A-S Medication Solutions
- Dosage form
- Tablet, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA090693
- Marketed since
- June 14, 2017
- 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 (3)
| Package NDC | Description | Since |
|---|---|---|
| 50090-4747-0 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-4747-0) | Nov 22, 2019 |
| 50090-4747-1 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-4747-1) | Nov 22, 2019 |
| 50090-4747-2 | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-4747-2) | Nov 22, 2019 |
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