NDC 70518-4056 – Bupropion Hydrochloride SR
Bupropion Hydrochloride 150 mg/1 · Tablet, Film Coated, Extended Release · Oral
Product NDC70518-4056
Product details
- Brand name
- Bupropion Hydrochloride SR
- Generic name
- Bupropion hydrochloride
- Labeler
- REMEDYREPACK INC.
- Dosage form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA205794
- Marketed since
- April 19, 2024
- 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 (1)
| Package NDC | Description | Since |
|---|---|---|
| 70518-4056-1 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (70518-4056-1) | Jan 23, 2025 |
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