Furosemide
- Product NDC
- 70934-737
- 11-digit product format
- 709340737
- Labeler code
- 70934
- Product ID
- 70934-737_a9da1637-32c1-708e-e053-2995a90ad553
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Furosemide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Denton Pharma, Inc. dba Northwind Pharmaceuticals
- Application
- NDA018823
- Marketing category
- NDA
- Marketing start
- 2020-05-22
- Marketing end
- 0000-00-00
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
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 | Marketing end | Sample | Exclude flag | Status |
|---|
| 70934-737-90 | 70934073790 | 90 TABLET in 1 BOTTLE, PLASTIC (70934-737-90) | 90 tablet | 2020-05-22 | 0000-00-00 | No | No | Current |