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
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Furosemide
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| FUROSEMIDE | 20 mg/2mL |
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 |
|---|
| 71872-7236-1 | Furosemide | 1 in 1 BAG | INJECTION, SOLUTION | 1 | | 2 |
| 71872-7236-1 | Furosemide | 2 mL in 1 VIAL | INJECTION, SOLUTION | 2 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71872-7236 | FUROSEMIDE INJECTION, SOLUTION [MEDICAL PURCHASING SOLUTIONS, LLC] | 2 | Current NDC, Legacy NDC, 2 package rows | 20230509_bbf03f9a-ae33-8da1-e053-2a95a90a3bdb.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | 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 | 0000-00-00 | No | No | Current |