FUROSEMIDE
- Product NDC
- 71872-7059
- 11-digit product format
- 718727059
- Labeler code
- 71872
- Product ID
- 71872-7059_fceaa3aa-c195-c32b-e053-6394a90a4ac5
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- furosemide
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Medical Purchasing Solutions, LLC
- Application
- ANDA202747
- Marketing category
- ANDA
- Marketing start
- 2014-02-06
- 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
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- FUROSEMIDE
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| FUROSEMIDE | 10 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 7LXU5N7ZO5 |
| Rxcui | 1719290 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 71872-7059-1 | FUROSEMIDE | 2 mL in 1 VIAL, GLASS | INJECTION, SOLUTION | 2 | | 3 |
| 71872-7059-1 | FUROSEMIDE | 1 in 1 BAG | INJECTION, SOLUTION | 1 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71872-7059 | FUROSEMIDE INJECTION, SOLUTION [MEDICAL PURCHASING SOLUTIONS, LLC] | 3 | Current NDC, Legacy NDC, 2 package rows | 20230531_6a2235e8-d488-2d43-e053-2991aa0aa485.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71872-7059-1 | 71872705901 | 1 VIAL, GLASS in 1 BAG (71872-7059-1) / 2 mL in 1 VIAL, GLASS | 2018-03-02 | 0000-00-00 | No | No | Current |