FUROSEMIDE
- Product NDC
- 52584-322
- 11-digit product format
- 525840322
- Labeler code
- 52584
- Product ID
- 52584-322_d5afe60e-2884-4446-a902-576e21b54711
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- furosemide
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- General Injectables & Vaccines, Inc.
- Application
- ANDA212174
- Marketing category
- ANDA
- Marketing start
- 2020-03-31
- Marketing end
- 2023-04-30
- Substance
- FUROSEMIDE
- Active strength
- 20 mg/2mL
- Pharmacologic classes
- Increased Diuresis at Loop of Henle [PE], Loop Diuretic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- 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 |
|---|
| 52584-322-01 | 52584032201 | 1 VIAL in 1 BAG (52584-322-01) > 2 mL in 1 VIAL | 1 vial | 2020-03-31 | 0000-00-00 | No | No | Current |