NDC 80425-0539 – Bupropion Hydrochloride (XL)
Bupropion Hydrochloride 300 mg/1 · Tablet, Film Coated, Extended Release · Oral
Product NDC80425-0539
Product details
- Brand name
- Bupropion Hydrochloride (XL)
- Generic name
- Bupropion hydrochloride
- Labeler
- Advanced Rx of Tennessee, LLC
- Dosage form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA207479
- Marketed since
- August 29, 2025
- Listing expires
- December 31, 2026
- Pharmacologic class
- Aminoketone
Active ingredients
- Bupropion Hydrochloride 300 mg/1
Uses, dosage, side effects and warnings for Bupropion hydrochloride →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 80425-0539-1 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (80425-0539-1) | Aug 29, 2025 |
| 80425-0539-2 | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (80425-0539-2) | Aug 29, 2025 |
| 80425-0539-3 | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (80425-0539-3) | Aug 29, 2025 |
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