Furosemide
- Product NDC
- 55154-2364
- 11-digit product format
- 551542364
- Labeler code
- 55154
- Product ID
- 55154-2364_f4d56261-4fb5-4876-b961-5927da951bcf
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Furosemide
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- Cardinal Health 107, LLC
- Application
- NDA018667
- Marketing category
- NDA
- Marketing start
- 2010-07-13
- 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
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Furosemide
- Listing expiration
- 2027-12-31
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 |
|---|
| 55154-2364-5 | Furosemide | 2 mL in 1 VIAL | INJECTION, SOLUTION | 2 | | 16 |
| 55154-2364-5 | Furosemide | 5 in 1 BAG | INJECTION, SOLUTION | 5 | | 16 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 55154-2364 | FUROSEMIDE INJECTION, SOLUTION [CARDINAL HEALTH 107, LLC] | 14 | Current NDC, Legacy NDC, 2 package rows | 20250101_8e0bac29-5a8b-4d4e-93b3-2e21eb3b0650.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 |
|---|
| 55154-2364-5 | 55154236405 | 5 VIAL in 1 BAG (55154-2364-5) / 2 mL in 1 VIAL | 5 vial | 2010-07-13 | 0000-00-00 | No | No | Current |