Furosemide
- Product NDC
- 72162-1360
- 11-digit product format
- 721621360
- Labeler code
- 72162
- Product ID
- 72162-1360_22202f87-ad58-420f-a081-22d646c8e7a8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- furosemide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA076796
- Marketing category
- ANDA
- Marketing start
- 2004-03-26
- 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
- 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 |
|---|
| 72162-1360-0 | 72162136000 | 1000 TABLET in 1 BOTTLE, PLASTIC (72162-1360-0) | 1000 tablet | 2024-02-02 | No | No | Historical |
| 72162-1360-1 | 72162136001 | 100 TABLET in 1 BOTTLE, PLASTIC (72162-1360-1) | 100 tablet | 2024-02-02 | No | No | Historical |