Furosemide
- Product NDC
- 70518-2528
- 11-digit product format
- 705182528
- Labeler code
- 70518
- Product ID
- 70518-2528_4a659a58-7fb2-57c1-e063-6394a90a4537
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Furosemide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA077293
- Marketing category
- ANDA
- Marketing start
- 2020-01-07
- Substance
- FUROSEMIDE
- Active strength
- 20 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 | 20 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 7LXU5N7ZO5 |
| Rxcui | 310429 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 70518-2528-0 | Furosemide | 5 in 1 BOTTLE, PLASTIC | TABLET | 5 | | 5 |
| 70518-2528-1 | Furosemide | 30 in 1 BLISTER PACK | TABLET | 30 | | 5 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 70518-2528-0 | 70518252800 | 5 in 1 BOTTLE, PLASTIC | | | | | Historical |
| 70518-2528-1 | 70518252801 | 30 TABLET in 1 BLISTER PACK (70518-2528-1) | 30 tablet | 2025-08-21 | No | No | Historical |