Furosemide
- Product NDC
- 50090-2713
- 11-digit product format
- 500902713
- Labeler code
- 50090
- Product ID
- 50090-2713_5c7ed6d6-e0b8-4df3-b454-f3401de5cd26
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Furosemide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA077293
- Marketing category
- ANDA
- Marketing start
- 2006-02-01
- 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, 313988 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50090-2713-0 | Furosemide | 100 in 1 BOTTLE | TABLET | 100 | | 19 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-2713 | FUROSEMIDE (FUROSEMIDE) TABLET [A-S MEDICATION SOLUTIONS] | 19 | Current NDC, Legacy NDC, 1 package rows | 20240425_83662449-f2b1-48a3-9021-13037e64e6ea.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 |
|---|
| 50090-2713-0 | 50090271300 | 100 TABLET in 1 BOTTLE (50090-2713-0) | 100 tablet | 2016-12-14 | 0000-00-00 | No | No | Current |