Furosemide
- Product NDC
- 71610-951
- 11-digit product format
- 716100951
- Labeler code
- 71610
- Product ID
- 71610-951_410bb6bd-91ef-1328-e063-6294a90a9dc9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Furosemide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Aphena Pharma Solutions - Tennessee, LLC
- Application
- ANDA077293
- Marketing category
- ANDA
- Marketing start
- 2006-02-01
- 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 |
|---|
| 71610-951-30 | 71610095130 | 30 TABLET in 1 BOTTLE (71610-951-30) | 30 tablet | 2025-10-13 | No | No | Historical |
| 71610-951-45 | 71610095145 | 45 TABLET in 1 BOTTLE (71610-951-45) | 45 tablet | 2025-09-19 | No | No | Historical |
| 71610-951-53 | 71610095153 | 60 TABLET in 1 BOTTLE (71610-951-53) | 60 tablet | 2025-09-19 | No | No | Historical |
| 71610-951-60 | 71610095160 | 90 TABLET in 1 BOTTLE (71610-951-60) | 90 tablet | 2025-09-19 | No | No | Historical |
| 71610-951-80 | 71610095180 | 180 TABLET in 1 BOTTLE (71610-951-80) | 180 tablet | 2025-09-19 | No | No | Historical |