Furosemide
- Product NDC
- 0054-4301
- 11-digit product format
- 000544301
- Labeler code
- 0054
- Product ID
- 0054-4301_bc62ddda-7639-4090-99f0-7dd4d13518f3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Furosemide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Hikma Pharmaceuticals USA Inc.
- Application
- ANDA070086
- Marketing category
- ANDA
- Marketing start
- 1991-03-13
- Substance
- FUROSEMIDE
- Active strength
- 80 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 | 80 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 7LXU5N7ZO5 |
| Rxcui | 197730, 197731, 197732, 310429, 313988 |
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
NDC, Effective, Action table| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|
| 0054-4301-25 | 2022-08-05 | C162847 | 48780-1 | e4f33bdf-a7a2-d8a0-e053-dadaa90a6e4e | Furosemide Tablets, USP and Furosemide Oral Solution, USP Rx only |
| 0054-4301-29 | 2022-08-05 | C162847 | 48780-1 | e4f33bdf-a7a2-d8a0-e053-dadaa90a6e4e | Furosemide Tablets, USP and Furosemide Oral Solution, USP Rx only |
| 0054-4301-25 | 2022-07-29 | C162847 | 48780-1 | e4f33bdf-a7a2-d8a0-e053-dadaa90a6e4e | Furosemide Tablets, USP and Furosemide Oral Solution, USP Rx only |
| 0054-4301-29 | 2022-07-29 | C162847 | 48780-1 | e4f33bdf-a7a2-d8a0-e053-dadaa90a6e4e | Furosemide Tablets, USP and Furosemide Oral Solution, USP Rx only |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 0054-4301-25 | Furosemide | 100 in 1 BOTTLE, PLASTIC | TABLET | 100 | | 18 |
| 0054-4301-29 | Furosemide | 500 in 1 BOTTLE, PLASTIC | TABLET | 500 | | 18 |
| 0054-4301-25 | Furosemide | 100 in 1 BOTTLE, PLASTIC | TABLET | 100 | | 1 |
| 0054-4301-29 | Furosemide | 500 in 1 BOTTLE, PLASTIC | TABLET | 500 | | 1 |
| 0054-8301-25 | Furosemide | 10 in 1 BOX | TABLET | 10 | | 1 |
| 0054-8301-25 | Furosemide | 100 in 1 BLISTER PACK | TABLET | 100 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0054-4301 | FUROSEMIDE TABLET FUROSEMIDE SOLUTION [HIKMA PHARMACEUTICALS USA INC.] | 16 | Current NDC, Legacy NDC, 2 package rows | 20250511_9e493331-dddd-496e-abf8-61747fb67aba.zip |
| 0054-4301 | FUROSEMIDE (FUROSEMIDE) TABLET FUROSEMIDE (FUROSEMIDE) SOLUTION [BOEHRINGER INGELHEIM PHARMACEUTICALS, INC.] | 1 | Current NDC, Legacy NDC, 4 package rows | 20070509_EA623E21-E9FD-4EF1-843B-82CBC05AF5BF.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 |
|---|
| 0054-4301-25 | 00054430125 | 100 TABLET in 1 BOTTLE, PLASTIC (0054-4301-25) | 100 tablet | 1991-03-13 | 0000-00-00 | No | No | Current |
| 0054-4301-29 | 00054430129 | 500 TABLET in 1 BOTTLE, PLASTIC (0054-4301-29) | 500 tablet | 1991-03-13 | 0000-00-00 | No | No | Current |
| 0054-8301-25 | 00054830125 | 10 in 1 BOX | | | | | | Historical |