NDC 0185-0128 – Bumetanide
Bumetanide .5 mg/1 · Tablet · Oral
Product NDC0185-0128
Product details
- Brand name
- Bumetanide
- Generic name
- Bumetanide
- Labeler
- Sandoz Inc
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA074700
- Marketed since
- November 21, 1996
- Listing expires
- December 31, 2026
- Pharmacologic class
- Loop Diuretic
Active ingredients
- Bumetanide .5 mg/1
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 0185-0128-01 | 100 TABLET in 1 BOTTLE (0185-0128-01) | Nov 21, 1996 |
| 0185-0128-05 | 500 TABLET in 1 BOTTLE (0185-0128-05) | Nov 21, 1996 |
Recalls mentioning this NDC
- D-341-2014 Dec 18, 2013 · Class III
Failed Moisture Limit; Out of Specification (OOS) results were obtained for moisture content during stability testing at the 12 month time point, controlled room temperature conditions.
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