Bumetanide
- Product NDC
- 0409-1412
- 11-digit product format
- 004091412
- Labeler code
- 0409
- Product ID
- 0409-1412_5d5a1e32-3392-489f-98c3-29f1f87711bc
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- BUMETANIDE
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- Hospira, Inc.
- Application
- ANDA074332
- Marketing category
- ANDA
- Marketing start
- 2006-07-06
- 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 |
|---|
| 0409-1412-04 | 00409141204 | 10 VIAL in 1 BOX (0409-1412-04) > 4 mL in 1 VIAL (0409-1412-34) | 10 vial | 2006-07-26 | 0000-00-00 | No | No | Current |
| 0409-1412-10 | 00409141210 | 10 VIAL, MULTI-DOSE in 1 BOX (0409-1412-10) > 10 mL in 1 VIAL, MULTI-DOSE (0409-1412-40) | | 2006-07-06 | 0000-00-00 | No | No | Current |