NDC 68682-580 – Bupropion Hydrobromide
Bupropion Hydrobromide 174 mg/1 · Tablet, Extended Release · Oral
Product NDC68682-580
Product details
- Brand name
- Bupropion Hydrobromide
- Generic name
- Bupropion Hydrobromide
- Labeler
- Oceanside Pharmaceuticals
- Dosage form
- Tablet, Extended Release
- Route
- Oral
- Marketing category
- NDA AUTHORIZED GENERIC · NDA022108
- Marketed since
- June 29, 2026
- Listing expires
- December 31, 2027
- Pharmacologic class
- Aminoketone
Active ingredients
- Bupropion Hydrobromide 174 mg/1
Uses, dosage, side effects and warnings for Bupropion Hydrobromide →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 68682-580-30 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68682-580-30) | Jun 29, 2026 |