Furosemide
- Product NDC
- 71610-843
- 11-digit product format
- 716100843
- Labeler code
- 71610
- Product ID
- 71610-843_dbc10744-27d9-46ad-9071-d5a049596b1c
- 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
- 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 |
|---|
| 71610-843-30 | 71610084330 | 30 TABLET in 1 BOTTLE (71610-843-30) | 30 tablet | 2024-06-26 | No | No | Historical |
| 71610-843-53 | 71610084353 | 60 TABLET in 1 BOTTLE (71610-843-53) | 60 tablet | 2024-06-26 | No | No | Historical |
| 71610-843-60 | 71610084360 | 90 TABLET in 1 BOTTLE (71610-843-60) | 90 tablet | 2024-06-26 | No | No | Historical |
| 71610-843-80 | 71610084380 | 180 TABLET in 1 BOTTLE (71610-843-80) | 180 tablet | 2024-06-26 | No | No | Historical |