Furosemide
- Product NDC
- 43353-737
- 11-digit product format
- 433530737
- Labeler code
- 43353
- Product ID
- 43353-737_3f914177-d57c-4f45-9cf3-4b98f8354ef8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Furosemide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Aphena Pharma Solutions - Tennessee, LLC
- Application
- NDA018569
- Marketing category
- NDA
- Marketing start
- 1981-10-19
- Marketing end
- 0000-00-00
- 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 7LXU5N7ZO5 | FUROSEMIDE | 54-31-9 | FUROSEMIDE |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Furosemide Tablets, USP | Aphena Pharma Solutions - Tennessee, LLC | 2014-05-12 | HUMAN PRESCRIPTION DRUG LABEL | 2 |