Furosemide
- Product NDC
- 64725-0624
- 11-digit product format
- 647250624
- Labeler code
- 64725
- Product ID
- 64725-0624_031a2a0f-f357-45ed-9719-67ed4c7bca8f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Furosemide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- TYA Pharmaceuticals
- Application
- ANDA078010
- Marketing category
- ANDA
- Marketing start
- 2009-01-29
- Marketing end
- 0000-00-00
- Substance
- FUROSEMIDE
- Active strength
- 20 mg/1
- Pharmacologic classes
- Increased Diuresis at Loop of Henle [PE],Loop Diuretic [EPC]
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| d80d3aff-3a63-4d7b-a2be-fd9388b04330 | Product name | 9 | 20250806 |
| 9061e89f-9c86-4196-b34b-886fc1673cc4 | Product name | 1 | 20140821 |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 64725-0624-1 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-0d12-f424-e053-dadaa90a57ce | Furosemide Tablets, USP Rx Only |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 64725-0624-1 | Furosemide | 100 in 1 BOTTLE | TABLET | 100 | 4 |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| FUROSEMIDE | ACTIVE INGREDIENT | 7LXU5N7ZO5 | FUROSEMIDE TABLET [TYA PHARMACEUTICALS] | 4 | |
| FUROSEMIDE | ACTIVE MOIETY | 7LXU5N7ZO5 | FUROSEMIDE TABLET [TYA PHARMACEUTICALS] | 4 | |
| LACTOSE MONOHYDRATE | INACTIVE INGREDIENT | EWQ57Q8I5X | FUROSEMIDE TABLET [TYA PHARMACEUTICALS] | 4 | |
| MAGNESIUM STEARATE | INACTIVE INGREDIENT | 70097M6I30 | FUROSEMIDE TABLET [TYA PHARMACEUTICALS] | 4 | |
| SODIUM STARCH GLYCOLATE TYPE A POTATO | INACTIVE INGREDIENT | 5856J3G2A2 | FUROSEMIDE TABLET [TYA PHARMACEUTICALS] | 4 | |
| STARCH, CORN | INACTIVE INGREDIENT | O8232NY3SJ | FUROSEMIDE TABLET [TYA PHARMACEUTICALS] | 4 | |
| WATER | INACTIVE INGREDIENT | 059QF0KO0R | FUROSEMIDE TABLET [TYA PHARMACEUTICALS] | 4 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 64725-0624 | FUROSEMIDE TABLET [TYA PHARMACEUTICALS] | 4 | Legacy NDC, 1 package rows | 20141027_d680e40c-5126-46dc-a44d-8ff95e66e920.zip |
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 310429 | furosemide 20 MG Oral Tablet | PSN | d680e40c-5126-46dc-a44d-8ff95e66e920 | 4 |
| 313988 | furosemide 40 MG Oral Tablet | PSN | d680e40c-5126-46dc-a44d-8ff95e66e920 | 4 |
| 310429 | furosemide 20 MG Oral Tablet | SCD | d680e40c-5126-46dc-a44d-8ff95e66e920 | 4 |
| 313988 | furosemide 40 MG Oral Tablet | SCD | d680e40c-5126-46dc-a44d-8ff95e66e920 | 4 |
Packages#
| Package NDC | 11-digit format | Description | Status |
|---|---|---|---|
| 64725-0624-1 | 64725062401 | 100 in 1 BOTTLE | Historical |