NDC 24979-248 – Bupropion hydrochloride
Bupropion Hydrochloride 450 mg/1 · Tablet, Film Coated, Extended Release · Oral
Product NDC24979-248
Product details
- Brand name
- Bupropion hydrochloride
- Generic name
- Bupropion hydrochloride
- Labeler
- Upsher-Smith Laboratories, LLC
- Dosage form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing category
- NDA AUTHORIZED GENERIC · NDA022497
- Marketed since
- December 15, 2023
- Listing expires
- December 31, 2027
- Pharmacologic class
- Aminoketone
Active ingredients
- Bupropion Hydrochloride 450 mg/1
Uses, dosage, side effects and warnings for Bupropion hydrochloride →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 24979-248-06 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (24979-248-06) | Dec 15, 2023 |
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