NDC 80425-0461 – Bupropion Hydrochloride
Bupropion Hydrochloride 150 mg/1 · Tablet, Extended Release · Oral
Product NDC80425-0461
Product details
- Brand name
- Bupropion Hydrochloride
- Generic name
- Bupropion Hydrochloride
- Labeler
- Advanced Rx of Tennessee, LLC
- Dosage form
- Tablet, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA210497
- Marketed since
- December 18, 2024
- 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 |
|---|---|---|
| 80425-0461-1 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (80425-0461-1) | Dec 18, 2024 |
| 80425-0461-2 | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (80425-0461-2) | Dec 18, 2024 |
| 80425-0461-3 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (80425-0461-3) | Dec 18, 2024 |
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