Furosemide
- Product NDC
- 52584-052
- 11-digit product format
- 525840052
- Labeler code
- 52584
- Product ID
- 52584-052_cf435438-0608-4411-9271-34e4ca22c83f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Furosemide
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- General Injectables & Vaccines, Inc.
- Application
- ANDA075241
- Marketing category
- ANDA
- Marketing start
- 2001-03-01
- 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
- 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 |
|---|
| 52584-052-10 | 52584005210 | 1 SYRINGE in 1 BAG (52584-052-10) > 10 mL in 1 SYRINGE | 1 syringe | 2010-03-01 | 0000-00-00 | No | No | Current |