Furosemide
- Product NDC
- 67046-222
- 11-digit product format
- 670460222
- Labeler code
- 67046
- Product ID
- 67046-222_aae04ef8-9438-43f4-9418-66b55d7bd7dc
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Furosemide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Contract Pharmacy Services-PA
- Application
- NDA018569
- Marketing category
- NDA
- Marketing start
- 2010-04-12
- 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
- E
- Listing certified through
- 2017-12-31
- 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 | Contract Pharmacy Services-PA | 2010-04-12 | HUMAN PRESCRIPTION DRUG LABEL | 1 |