NDC 68788-8769 – Bupropion hydrochloride
Bupropion Hydrochloride 150 mg/1 · Tablet, Extended Release · Oral
Product NDC68788-8769
Product details
- Brand name
- Bupropion hydrochloride
- Generic name
- Bupropion hydrochloride
- Labeler
- Preferred Pharmaceuticals Inc.
- Dosage form
- Tablet, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA216800
- Marketed since
- November 19, 2024
- Listing expires
- December 31, 2027
- Pharmacologic class
- Aminoketone
Active ingredients
- Bupropion Hydrochloride 150 mg/1
Uses, dosage, side effects and warnings for Bupropion hydrochloride →
Package NDC codes (6)
| Package NDC | Description | Since |
|---|---|---|
| 68788-8769-1 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8769-1) | Nov 19, 2024 |
| 68788-8769-2 | 20 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8769-2) | Nov 19, 2024 |
| 68788-8769-3 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8769-3) | Nov 19, 2024 |
| 68788-8769-6 | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8769-6) | Nov 19, 2024 |
| 68788-8769-8 | 120 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8769-8) | Nov 19, 2024 |
| 68788-8769-9 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8769-9) | Nov 19, 2024 |
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