FUROSEMIDE
- Product NDC
- 61919-242
- 11-digit product format
- 619190242
- Labeler code
- 61919
- Product ID
- 61919-242_eac39a9f-9e73-3866-e053-2a95a90a5768
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- FUROSEMIDE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- DIRECT RX
- Application
- ANDA077293
- Marketing category
- ANDA
- Marketing start
- 2020-06-18
- 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
- 2027-12-31
- Current FDA listing
- Yes
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 | Sample | Exclude flag | Status |
|---|
| 61919-242-30 | 61919024230 | 30 TABLET in 1 BOTTLE (61919-242-30) | 30 tablet | 2020-06-18 | No | No | Historical |
| 61919-242-90 | 61919024290 | 90 TABLET in 1 BOTTLE (61919-242-90) | 90 tablet | 2020-06-18 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| FUROSEMIDE | DIRECT RX | 2024-01-09 | HUMAN PRESCRIPTION DRUG LABEL | 6 |