Furosemide
- Product NDC
- 42708-123
- 11-digit product format
- 427080123
- Labeler code
- 42708
- Product ID
- 42708-123_459c0c80-5889-208c-e063-6294a90a4d0d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Furosemide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- QPharma Inc
- Application
- ANDA077293
- Marketing category
- ANDA
- Marketing start
- 2006-02-01
- Substance
- FUROSEMIDE
- Active strength
- 40 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 | 40 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 7LXU5N7ZO5 |
| Rxcui | 313988 |
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 42708-123-30 | Furosemide | 30 in 1 BOTTLE | TABLET | 30 | | 6 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 42708-123 | FUROSEMIDE TABLET [QPHARMA INC] | 5 | Current NDC, Legacy NDC, 1 package rows | 20241123_341e29d9-a6f1-4c77-ae44-9b2c423ea6b4.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 |
|---|
| 42708-123-30 | 42708012330 | 30 TABLET in 1 BOTTLE (42708-123-30) | 30 tablet | 2018-05-23 | 0000-00-00 | Yes | No | Current |