NDC 70518-4218 – Bupropion Hydrochloride
Bupropion Hydrochloride 100 mg/1 · Tablet, Film Coated · Oral
Product NDC70518-4218
Product details
- Brand name
- Bupropion Hydrochloride
- Generic name
- Bupropion Hydrochloride
- Labeler
- REMEDYREPACK INC.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA203013
- Marketed since
- October 21, 2024
- Listing expires
- December 31, 2027
- Pharmacologic class
- Aminoketone
Active ingredients
- Bupropion Hydrochloride 100 mg/1
Uses, dosage, side effects and warnings for Bupropion hydrochloride →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 70518-4218-0 | 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4218-0) | Oct 21, 2024 |
| 70518-4218-1 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4218-1) | Jan 8, 2026 |
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