NDC 71610-899 – Bupropion Hydrochloride
Bupropion Hydrochloride 75 mg/1 · Tablet · Oral
Product NDC71610-899
Product details
- Brand name
- Bupropion Hydrochloride
- Generic name
- Bupropion Hydrochloride
- Labeler
- Aphena Pharma Solutions - Tennessee, LLC
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA206975
- Marketed since
- January 30, 2025
- Listing expires
- December 31, 2027
- Pharmacologic class
- Aminoketone
Active ingredients
- Bupropion Hydrochloride 75 mg/1
Uses, dosage, side effects and warnings for Bupropion hydrochloride →
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 71610-899-42 | 1800 TABLET in 1 BOTTLE (71610-899-42) | Aug 24, 2026 |
| 71610-899-53 | 60 TABLET in 1 BOTTLE (71610-899-53) | Apr 15, 2025 |
| 71610-899-60 | 90 TABLET in 1 BOTTLE (71610-899-60) | Apr 15, 2025 |
| 71610-899-80 | 180 TABLET in 1 BOTTLE (71610-899-80) | Apr 15, 2025 |
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