NDC 60687-782 – Bupropion Hydrochloride
Bupropion Hydrochloride 150 mg/1 · Tablet, Extended Release · Oral
Product NDC60687-782
Product details
- Brand name
- Bupropion Hydrochloride
- Generic name
- Bupropion Hydrochloride
- Labeler
- American Health Packaging
- Dosage form
- Tablet, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA090693
- Marketed since
- January 15, 2024
- Listing expires
- December 31, 2026
- Pharmacologic class
- Aminoketone
Active ingredients
- Bupropion Hydrochloride 150 mg/1
Uses, dosage, side effects and warnings for Bupropion hydrochloride →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 60687-782-01 | 100 BLISTER PACK in 1 CARTON (60687-782-01) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (60687-782-11) | Jan 15, 2024 |
Recalls mentioning this NDC
- D-0590-2024 Jul 17, 2024 · Class II
Failed Dissolution Specifications; the product is dissolving faster than the specified limits.
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