Furosemide
- Product NDC
- 55154-2348
- 11-digit product format
- 551542348
- Labeler code
- 55154
- Product ID
- 55154-2348_392096c5-3e3f-47c0-b793-54392f17ccf8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- furosemide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Cardinal Health 107, LLC
- Application
- ANDA076796
- Marketing category
- ANDA
- Marketing start
- 2024-12-04
- Substance
- FUROSEMIDE
- Active strength
- 40 mg/1
- 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 | 40 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 7LXU5N7ZO5 |
| Rxcui | 310429, 313988 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 55154-2348-0 | Furosemide | 1 in 1 BLISTER PACK | TABLET | 1 | | 3 |
| 55154-2348-0 | Furosemide | 10 in 1 BAG | TABLET | 10 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 55154-2348 | FUROSEMIDE TABLET [CARDINAL HEALTH 107, LLC] | 3 | Current NDC, 2 package rows | 20250507_2a5bcf50-6d63-463a-915e-a72ea2e5f131.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 55154-2348-0 | 55154234800 | 10 BLISTER PACK in 1 BAG (55154-2348-0) / 1 TABLET in 1 BLISTER PACK | 10 blister pack | 2024-12-04 | No | No | Historical |