Furosemide
- Product NDC
- 71872-7236
- 11-digit product format
- 718727236
- Labeler code
- 71872
- Product ID
- 71872-7236_fb32ee8a-091d-2153-e053-6394a90ae9a8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Furosemide
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- Medical Purchasing Solutions, LLC
- Application
- ANDA212174
- Marketing category
- ANDA
- Marketing start
- 2019-05-03
- Substance
- FUROSEMIDE
- Active strength
- 20 mg/2mL
- 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 |
|---|
| 71872-7236-1 | 71872723601 | 1 VIAL in 1 BAG (71872-7236-1) / 2 mL in 1 VIAL | 1 vial | 2020-12-15 | No | No | Historical |