Furosemide
- Product NDC
- 50090-4109
- 11-digit product format
- 500904109
- Labeler code
- 50090
- Product ID
- 50090-4109_54ca7b79-abef-40ad-b224-0bf2d5affbfb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Furosemide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- NDA018823
- Marketing category
- NDA
- Marketing start
- 1983-11-10
- 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
- 2020-12-31
- 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 |
|---|
| 50090-4109-0 | 50090410900 | 30 TABLET in 1 BOTTLE (50090-4109-0) | 30 tablet | 2019-02-01 | 0000-00-00 | No | No | Current |