NDC 70518-3790 – Bupropion Hydrochloride (XL)
Bupropion Hydrochloride 300 mg/1 · Tablet, Film Coated, Extended Release · Oral
Product NDC70518-3790
Product details
- Brand name
- Bupropion Hydrochloride (XL)
- Generic name
- Bupropion hydrochloride
- Labeler
- REMEDYREPACK INC.
- Dosage form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA207479
- Marketed since
- July 13, 2023
- Listing expires
- December 31, 2027
- Pharmacologic class
- Aminoketone
Active ingredients
- Bupropion Hydrochloride 300 mg/1
Uses, dosage, side effects and warnings for Bupropion hydrochloride →
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 70518-3790-1 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-3790-1) | Jun 7, 2024 |
| 70518-3790-2 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (70518-3790-2) | Mar 20, 2026 |
| 70518-3790-3 | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-3790-3) | Apr 15, 2026 |
| 70518-3790-4 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (70518-3790-4) | Jul 20, 2026 |
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