NDC 67046-1572 – Bupropion hydrochloride
Bupropion Hydrochloride 100 mg/1 · Tablet, Extended Release · Oral
Product NDC67046-1572
Product details
- Brand name
- Bupropion hydrochloride
- Generic name
- Bupropion hydrochloride
- Labeler
- Coupler LLC
- Dosage form
- Tablet, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA216800
- Marketed since
- July 2, 2025
- Listing expires
- December 31, 2026
- Pharmacologic class
- Aminoketone
Active ingredients
- Bupropion Hydrochloride 100 mg/1
Uses, dosage, side effects and warnings for Bupropion hydrochloride →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 67046-1572-3 | 30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (67046-1572-3) | Jul 2, 2025 |
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