NDC 70518-4674 – Bupropion hydrochloride
Bupropion Hydrochloride 150 mg/1 · Tablet, Extended Release · Oral
Product NDC70518-4674
Product details
- Brand name
- Bupropion hydrochloride
- Generic name
- Bupropion hydrochloride
- Labeler
- REMEDYREPACK INC.
- Dosage form
- Tablet, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA211020
- Marketed since
- June 2, 2026
- 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 (2)
| Package NDC | Description | Since |
|---|---|---|
| 70518-4674-0 | 30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (70518-4674-0) | Jun 2, 2026 |
| 70518-4674-1 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-4674-1) | Sep 2, 2026 |
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