Furosemide
- Product NDC
- 71872-7350
- 11-digit product format
- 718727350
- Labeler code
- 71872
- Product ID
- 71872-7350_4227facb-527f-27ae-e063-6294a90a65fb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Furosemide
- Dosage form
- INJECTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- Medical Purchasing Solutions, LLC.
- Application
- NDA018267
- Marketing category
- NDA
- Marketing start
- 2024-08-19
- 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 | Marketing start | Sample | Exclude flag | Status |
|---|
| 71872-7350-1 | 71872735001 | 1 VIAL, SINGLE-DOSE in 1 BAG (71872-7350-1) / 10 mL in 1 VIAL, SINGLE-DOSE | 2025-05-05 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Furosemide | Medical Purchasing Solutions, LLC. | 2025-10-27 | HUMAN PRESCRIPTION DRUG LABEL | 1 |