Furosemide
- Product NDC
- 50090-4109
- 11-digit product format
- 500904109
- Labeler code
- 50090
- Product ID
- 50090-4109_54ca7b79-abef-40ad-b224-0bf2d5affbfb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Furosemide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- NDA018823
- Marketing category
- NDA
- Marketing start
- 1983-11-10
- Marketing end
- 0000-00-00
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
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 |
|---|
| 50090-4109-0 | Furosemide | 30 in 1 BOTTLE | TABLET | 30 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-4109 | FUROSEMIDE TABLET [A-S MEDICATION SOLUTIONS] | 2 | Legacy NDC, 1 package rows | 20190205_794c145d-660d-4541-9e01-e72de70be543.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 |
|---|
| 50090-4109-0 | 50090410900 | 30 TABLET in 1 BOTTLE (50090-4109-0) | 30 tablet | 2019-02-01 | 0000-00-00 | No | No | Current |