Furosemide
- Product NDC
- 50090-7705
- 11-digit product format
- 500907705
- Labeler code
- 50090
- Product ID
- 50090-7705_14f13cca-689e-4468-a940-4d45a223cd11
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Furosemide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA078010
- Marketing category
- ANDA
- Marketing start
- 2024-06-03
- 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
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 7LXU5N7ZO5 | FUROSEMIDE | 54-31-9 | FUROSEMIDE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 50090-7705-0 | 50090770500 | 90 TABLET in 1 BOTTLE (50090-7705-0) | 90 tablet | 2025-10-14 | No | No | Historical |