NDC 68788-4010 – Bupropion hydrochloride
Bupropion Hydrochloride 150 mg/1 · Tablet, Extended Release · Oral
Product NDC68788-4010
Product details
- Brand name
- Bupropion hydrochloride
- Generic name
- Bupropion hydrochloride
- Labeler
- Preferred Pharmaceuticals Inc.
- Dosage form
- Tablet, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA215568
- Marketed since
- September 4, 2025
- Listing expires
- December 31, 2026
- Pharmacologic class
- Aminoketone
Active ingredients
- Bupropion Hydrochloride 150 mg/1
Uses, dosage, side effects and warnings for Bupropion hydrochloride →
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 68788-4010-1 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-4010-1) | Sep 4, 2025 |
| 68788-4010-3 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-4010-3) | Sep 4, 2025 |
| 68788-4010-6 | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-4010-6) | Sep 4, 2025 |
| 68788-4010-9 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-4010-9) | Sep 4, 2025 |
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