NDC 50090-7422 – Bupropion hydrochloride
Bupropion Hydrochloride 150 mg/1 · Tablet, Extended Release · Oral
Product NDC50090-7422
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 · ANDA216800
- Marketed since
- May 31, 2023
- 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 (4)
| Package NDC | Description | Since |
|---|---|---|
| 50090-7422-0 | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-7422-0) | Oct 28, 2024 |
| 50090-7422-1 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-7422-1) | Oct 28, 2024 |
| 50090-7422-2 | 180 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-7422-2) | Oct 28, 2024 |
| 50090-7422-3 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-7422-3) | Oct 28, 2024 |
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