NDC 71610-866 – bupropion Hydrochloride
Bupropion Hydrochloride 75 mg/1 · Tablet · Oral
Product NDC71610-866
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
- August 19, 2016
- Listing expires
- December 31, 2026
- 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 |
|---|---|---|
| 71610-866-53 | 60 TABLET in 1 BOTTLE (71610-866-53) | Nov 21, 2024 |
| 71610-866-60 | 90 TABLET in 1 BOTTLE (71610-866-60) | Nov 21, 2024 |
| 71610-866-70 | 120 TABLET in 1 BOTTLE (71610-866-70) | Nov 21, 2024 |
| 71610-866-80 | 180 TABLET in 1 BOTTLE (71610-866-80) | Nov 21, 2024 |
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