FUROSEMIDE
- Product NDC
- 0409-1639
- 11-digit product format
- 004091639
- Labeler code
- 0409
- Product ID
- 0409-1639_9fbc6985-64fd-4233-b401-8097a3895b8c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- furosemide
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- Hospira, Inc.
- Application
- ANDA075241
- Marketing category
- ANDA
- Marketing start
- 2006-01-31
- Marketing end
- 0000-00-00
- Substance
- FUROSEMIDE
- Active strength
- 10 mg/mL
- Pharmacologic classes
- Increased Diuresis at Loop of Henle [PE], Loop Diuretic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 0409-1639-10 | 00409163910 | 10 CARTON in 1 PACKAGE (0409-1639-10) > 1 SYRINGE, PLASTIC in 1 CARTON (0409-1639-21) > 10 mL in 1 SYRINGE, PLASTIC | 10 carton | 2006-01-31 | 0000-00-00 | No | No | Current |