Furosemide
- Product NDC
- 71335-0852
- 11-digit product format
- 713350852
- Labeler code
- 71335
- Product ID
- 71335-0852_14d6a850-12a9-4c10-bd7c-1c1acf500d56
- 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 |
|---|
| 71335-0852-1 | 71335085201 | 30 TABLET in 1 BOTTLE (71335-0852-1) | 30 tablet | 2018-06-22 | No | No | Historical |
| 71335-0852-2 | 71335085202 | 90 TABLET in 1 BOTTLE (71335-0852-2) | 90 tablet | 2018-06-22 | No | No | Historical |
| 71335-0852-3 | 71335085203 | 60 TABLET in 1 BOTTLE (71335-0852-3) | 60 tablet | 2018-06-22 | No | No | Historical |
| 71335-0852-4 | 71335085204 | 100 TABLET in 1 BOTTLE (71335-0852-4) | 100 tablet | 2018-06-22 | No | No | Historical |
| 71335-0852-5 | 71335085205 | 7 TABLET in 1 BOTTLE (71335-0852-5) | 7 tablet | 2018-06-22 | No | No | Historical |
| 71335-0852-6 | 71335085206 | 28 TABLET in 1 BOTTLE (71335-0852-6) | 28 tablet | 2018-06-22 | No | No | Historical |
| 71335-0852-7 | 71335085207 | 14 TABLET in 1 BOTTLE (71335-0852-7) | 14 tablet | 2018-06-22 | No | No | Historical |
| 71335-0852-8 | 71335085208 | 10 TABLET in 1 BOTTLE (71335-0852-8) | 10 tablet | 2018-06-22 | No | No | Historical |
| 71335-0852-9 | 71335085209 | 20 TABLET in 1 BOTTLE (71335-0852-9) | 20 tablet | 2018-06-22 | No | No | Historical |