NDC 31722-487 – Bupropion Hydrochloride
Bupropion Hydrochloride 150 mg/1 · Tablet, Extended Release · Oral
Product NDC31722-487
Product details
- Brand name
- Bupropion Hydrochloride
- Generic name
- Bupropion Hydrochloride
- Labeler
- Camber Pharmaceuticals, Inc.
- Dosage form
- Tablet, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA217898
- Marketed since
- October 1, 2025
- 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 (3)
| Package NDC | Description | Since |
|---|---|---|
| 31722-487-05 | 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (31722-487-05) | Oct 1, 2025 |
| 31722-487-30 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (31722-487-30) | Oct 1, 2025 |
| 31722-487-90 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (31722-487-90) | Oct 1, 2025 |
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