NDC 68788-7992 – Bupropion Hydrochloride
Bupropion Hydrochloride 300 mg/1 · Tablet, Extended Release · Oral
Product NDC68788-7992
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
- August 6, 2021
- Listing expires
- December 31, 2026
- Pharmacologic class
- Aminoketone
Active ingredients
- Bupropion Hydrochloride 300 mg/1
Uses, dosage, side effects and warnings for Bupropion hydrochloride →
Package NDC codes (5)
| Package NDC | Description | Since |
|---|---|---|
| 68788-7992-1 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-7992-1) | Aug 6, 2021 |
| 68788-7992-3 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-7992-3) | Aug 6, 2021 |
| 68788-7992-6 | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-7992-6) | Aug 6, 2021 |
| 68788-7992-8 | 120 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-7992-8) | Aug 6, 2021 |
| 68788-7992-9 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-7992-9) | Aug 6, 2021 |
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