Furosemide
- Product NDC
- 55154-5875
- 11-digit product format
- 551545875
- Labeler code
- 55154
- Product ID
- 55154-5875_a4453a71-622c-4887-8e9d-37d08d656b2b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Furosemide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Cardinal Health
- Application
- NDA018569
- Marketing category
- NDA
- Marketing start
- 2008-03-26
- Marketing end
- 2019-06-30
- 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
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 7LXU5N7ZO5 | FUROSEMIDE | 54-31-9 | FUROSEMIDE |