Furosemide
- Product NDC
- 61919-255
- 11-digit product format
- 619190255
- Labeler code
- 61919
- Product ID
- 61919-255_4c9831b2-708e-dcf2-e063-6394a90ad5fc
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Furosemide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Direct_Rx
- Application
- ANDA077293
- Marketing category
- ANDA
- Marketing start
- 2021-10-21
- 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
- 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 | 40 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 7LXU5N7ZO5 |
| Rxcui | 313988 |
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 61919-255-30 | Furosemide | 30 in 1 BOTTLE | TABLET | 30 | | 2 |
| 61919-255-90 | Furosemide | 90 in 1 BOTTLE | TABLET | 90 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 61919-255 | FUROSEMIDE TABLET [DIRECT_RX] | 1 | Current NDC, Legacy NDC, 2 package rows | 20220929_e9be5c3b-4b18-7ad2-e053-2995a90a4a8b.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 |
|---|
| 61919-255-30 | 61919025530 | 30 TABLET in 1 BOTTLE (61919-255-30) | 30 tablet | 2021-10-21 | | No | No | Historical |
| 61919-255-90 | 61919025590 | 90 TABLET in 1 BOTTLE (61919-255-90) | 90 tablet | 2021-10-21 | 0000-00-00 | No | No | Current |