Furosemide
- Product NDC
- 68071-3673
- 11-digit product format
- 680713673
- Labeler code
- 68071
- Product ID
- 68071-3673_414d2cef-c3a6-7fdb-e063-6394a90a01d1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Furosemide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals, Inc.
- Application
- ANDA216629
- Marketing category
- ANDA
- Marketing start
- 2022-11-05
- 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
- 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 | 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 |
|---|
| 68071-3673-3 | Furosemide | 30 in 1 BOTTLE | TABLET | 30 | | 2 |
| 68071-3673-9 | 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 |
|---|
| 68071-3673 | FUROSEMIDE TABLET [NUCARE PHARMACEUTICALS, INC.] | 1 | Current NDC, 2 package rows | 20240901_20eecc36-dfb7-0060-e063-6394a90a9d0b.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 68071-3673-3 | 68071367303 | 30 TABLET in 1 BOTTLE (68071-3673-3) | 30 tablet | 2024-08-30 | No | No | Current |
| 68071-3673-9 | 68071367309 | 90 TABLET in 1 BOTTLE (68071-3673-9) | 90 tablet | 2025-10-16 | No | No | Current |