FUROSEMIDE
- Product NDC
- 51662-1572
- 11-digit product format
- 516621572
- Labeler code
- 51662
- Product ID
- 51662-1572_0f907fa8-d143-b8c3-e063-6394a90a1a2e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- FUROSEMIDE
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- HF Acquisition Co LLC, DBA HealthFirst
- Application
- NDA018902
- Marketing category
- NDA
- Marketing start
- 2021-06-28
- Substance
- FUROSEMIDE
- Active strength
- 10 mg/mL
- Pharmacologic classes
- Increased Diuresis at Loop of Henle [PE], Loop Diuretic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- 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 |
|---|
| 51662-1572-1 | 51662157201 | 2 mL in 1 VIAL (51662-1572-1) | 2 ml | 2021-06-28 | No | No | Historical |
| 51662-1572-3 | 51662157203 | 25 POUCH in 1 CASE (51662-1572-3) / 1 VIAL in 1 POUCH (51662-1572-2) / 2 mL in 1 VIAL | 25 pouch | 2022-06-12 | No | No | Historical |