Furosemide
- Product NDC
- 52584-283
- 11-digit product format
- 525840283
- Labeler code
- 52584
- Product ID
- 52584-283_401b0e37-d9fa-48c6-ba97-8dd7a7c0cd56
- 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
- 2023-12-31
- 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 |
|---|
| 52584-283-25 | 52584028325 | 1 VIAL, SINGLE-DOSE in 1 BAG (52584-283-25) > 4 mL in 1 VIAL, SINGLE-DOSE | 2019-06-04 | 0000-00-00 | No | No | Current |