NDC 80425-0300 – Bupropion hydrochloride
Bupropion Hydrochloride 150 mg/1 · Tablet, Extended Release · Oral
Product NDC80425-0300
Product details
- Brand name
- Bupropion hydrochloride
- Generic name
- Bupropion hydrochloride
- Labeler
- Advanced Rx Pharmacy of Tennessee, LLC
- Dosage form
- Tablet, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA210497
- Marketed since
- April 6, 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 (3)
| Package NDC | Description | Since |
|---|---|---|
| 80425-0300-1 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (80425-0300-1) | Apr 6, 2023 |
| 80425-0300-2 | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (80425-0300-2) | Apr 6, 2023 |
| 80425-0300-3 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (80425-0300-3) | Apr 6, 2023 |
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