Bumetanide
- Product NDC
- 55154-4733
- 11-digit product format
- 551544733
- Labeler code
- 55154
- Product ID
- 55154-4733_d0c62771-71c4-4748-99d4-a476a0571951
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- BUMETANIDE
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- Cardinal Health
- Application
- ANDA074332
- Marketing category
- ANDA
- Marketing start
- 2011-11-16
- Marketing end
- 0000-00-00
- Substance
- BUMETANIDE
- Active strength
- 0 mg/mL
- Pharmacologic classes
- Loop Diuretic [EPC],Increased Diuresis at Loop of Henle [PE]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55154-4733-5 | 55154473305 | 5 VIAL in 1 BAG (55154-4733-5) > 4 mL in 1 VIAL | 5 vial | 2011-11-16 | 0000-00-00 | No | No | Current |