Furosemide
- Product NDC
- 51079-072
- 11-digit product format
- 510790072
- Labeler code
- 51079
- Product ID
- 51079-072_d347d4b5-8000-f23e-e053-2a95a90a9ad0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- furosemide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Mylan Institutional Inc.
- Application
- NDA018487
- Marketing category
- NDA
- Marketing start
- 1997-02-06
- Marketing end
- 2030-01-31
- Substance
- FUROSEMIDE
- Active strength
- 20 mg/1
- 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 |
|---|
| 51079-072-20 | 51079007220 | 100 BLISTER PACK in 1 CARTON (51079-072-20) > 1 TABLET in 1 BLISTER PACK (51079-072-01) | 100 blister pack | 1997-02-06 | 0000-00-00 | No | No | Current |