NDC 31722-066 – Bupropion hydrochloride
Bupropion Hydrochloride 100 mg/1 · Tablet, Extended Release · Oral
Product NDC31722-066
Product details
- Brand name
- Bupropion hydrochloride
- Generic name
- Bupropion hydrochloride
- Labeler
- Camber Pharmaceuticals, Inc.
- Dosage form
- Tablet, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA216800
- Marketed since
- May 31, 2023
- Listing expires
- December 31, 2027
- Pharmacologic class
- Aminoketone
Active ingredients
- Bupropion Hydrochloride 100 mg/1
Uses, dosage, side effects and warnings for Bupropion hydrochloride →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 31722-066-01 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (31722-066-01) | May 31, 2023 |
| 31722-066-05 | 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (31722-066-05) | May 31, 2023 |
| 31722-066-60 | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (31722-066-60) | May 31, 2023 |
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