FUROSEMIDE
- Product NDC
- 52584-284
- 11-digit product format
- 525840284
- Labeler code
- 52584
- Product ID
- 52584-284_a1825ebc-0f66-4a97-b53d-ccf58f053164
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- furosemide
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- General Injectables & Vaccines, Inc.
- Application
- ANDA202747
- Marketing category
- ANDA
- Marketing start
- 2019-08-15
- Marketing end
- 2023-11-30
- 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 |
|---|
| 52584-284-25 | 52584028425 | 1 VIAL, GLASS in 1 BAG (52584-284-25) > 1 mL in 1 VIAL, GLASS | 2019-08-15 | 0000-00-00 | No | No | Current |