Furosemide
- Product NDC
- 52584-091
- 11-digit product format
- 525840091
- Labeler code
- 52584
- Product ID
- 52584-091_a18b4fe3-baa3-4721-98c1-b9cf7d334ec3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Furosemide
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- General Injectables and Vaccines, Inc.
- Application
- ANDA202747
- Marketing category
- ANDA
- Marketing start
- 2019-06-04
- Marketing end
- 2021-12-31
- 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
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 52584-091-25 | 52584009125 | 1 VIAL, SINGLE-DOSE in 1 BAG (52584-091-25) > 2 mL in 1 VIAL, SINGLE-DOSE | 2019-06-04 | 2021-12-31 | No | No | Current |