FUROSEMIDE
- Product NDC
- 59651-798
- 11-digit product format
- 596510798
- Labeler code
- 59651
- Product ID
- 59651-798_a504ee4b-3995-45f2-898c-91116dd81d19
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- FUROSEMIDE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Aurobindo Pharma Limited
- Application
- ANDA218831
- Marketing category
- ANDA
- Marketing start
- 2025-07-17
- 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
- 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 | 80 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 7LXU5N7ZO5 |
| Rxcui | 197732, 310429, 313988 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 59651-798-01 | FUROSEMIDE | 100 in 1 BOTTLE | TABLET | 100 | | 1 |
| 59651-798-05 | FUROSEMIDE | 500 in 1 BOTTLE | TABLET | 500 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 59651-798-01 | 59651079801 | 100 TABLET in 1 BOTTLE (59651-798-01) | 100 tablet | 2025-07-17 | No | No | Current |
| 59651-798-05 | 59651079805 | 500 TABLET in 1 BOTTLE (59651-798-05) | 500 tablet | 2025-07-17 | No | No | Current |
| 59651-798-62 | 59651079862 | 30000 TABLET in 1 BAG (59651-798-62) | 30000 tablet | 17-JUL-25 | | | Current |