Furosemide
- Product NDC
- 50090-3455
- 11-digit product format
- 500903455
- Labeler code
- 50090
- Product ID
- 50090-3455_de46400f-13ed-487d-ae10-4eb239dd4596
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- furosemide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA076796
- Marketing category
- ANDA
- Marketing start
- 2004-03-26
- Marketing end
- 0000-00-00
- Substance
- FUROSEMIDE
- Active strength
- 40 mg/1
- Pharmacologic classes
- Increased Diuresis at Loop of Henle [PE],Loop Diuretic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-3455-1 | 50090345501 | 180 TABLET in 1 BOTTLE (50090-3455-1) | 180 tablet | 2018-05-15 | 0000-00-00 | No | No | Current |