NDC 68788-7786 – Bupropion Hydrochloride
Bupropion Hydrochloride 150 mg/1 · Tablet, Extended Release · Oral
Product NDC68788-7786
Product details
- Brand name
- Bupropion Hydrochloride
- Generic name
- Bupropion Hydrochloride
- Labeler
- Preferred Pharmaceuticals Inc.
- Dosage form
- Tablet, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA210497
- Marketed since
- October 21, 2020
- 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 (5)
| Package NDC | Description | Since |
|---|---|---|
| 68788-7786-1 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-7786-1) | Oct 21, 2020 |
| 68788-7786-3 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-7786-3) | Oct 21, 2020 |
| 68788-7786-6 | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-7786-6) | Oct 21, 2020 |
| 68788-7786-8 | 120 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-7786-8) | Oct 21, 2020 |
| 68788-7786-9 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-7786-9) | Oct 21, 2020 |
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