Furosemide
- Product NDC
- 55154-2365
- 11-digit product format
- 551542365
- Labeler code
- 55154
- Product ID
- 55154-2365_8bc0d5e5-a546-408b-9f55-b68baa06b507
- 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
- 2005-02-28
- 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 | 1719291 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 55154-2365-5 | Furosemide | 4 mL in 1 VIAL, SINGLE-USE | INJECTION, SOLUTION | 4 | | 18 |
| 55154-2365-5 | Furosemide | 5 in 1 BAG | INJECTION, SOLUTION | 5 | | 18 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 55154-2365 | FUROSEMIDE INJECTION, SOLUTION [CARDINAL HEALTH 107, LLC] | 16 | Current NDC, Legacy NDC, 2 package rows | 20250105_71b48f4d-9936-448c-9e3a-33f1182e1039.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 |
|---|
| 55154-2365-5 | 55154236505 | 5 VIAL, SINGLE-USE in 1 BAG (55154-2365-5) / 4 mL in 1 VIAL, SINGLE-USE | 2005-02-28 | 0000-00-00 | No | No | Current |