NDC 0832-0541 – Bumetanide
Bumetanide 1 mg/1 · Tablet · Oral
Product NDC0832-0541
Product details
- Brand name
- Bumetanide
- Generic name
- Bumetanide
- Labeler
- Upsher-Smith Laboratories, LLC
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA209916
- Marketed since
- January 30, 2018
- Marketing end
- September 30, 2026
- Pharmacologic class
- Loop Diuretic
Active ingredients
- Bumetanide 1 mg/1
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 0832-0541-10 | 1000 TABLET in 1 BOTTLE (0832-0541-10) | Jan 30, 2018 |
| 0832-0541-11 | 100 TABLET in 1 BOTTLE (0832-0541-11) | Jan 30, 2018 |
Recalls mentioning this NDC
- D-0280-2019 Oct 31, 2018 · Class II
Failed impurities/ degradation specifications: Product is Out of Specification for an unspecified degradation product. - D-0281-2019 Oct 31, 2018 · Class II
Failed impurities/ degradation specifications: Product is Out of Specification for an unspecified degradation product.
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