Furosemide
- Product NDC
- 53808-1109
- 11-digit product format
- 538081109
- Labeler code
- 53808
- Product ID
- 53808-1109_0349dc51-00b4-4f90-ba8d-0590a7098610
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- furosemide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- DOH CENTRAL PHARMACY
- Application
- ANDA076796
- Marketing category
- ANDA
- Marketing start
- 2018-04-25
- 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 |
|---|
| 53808-1109-1 | Furosemide | 30 in 1 BLISTER PACK | TABLET | 30 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 53808-1109 | FUROSEMIDE TABLET [DOH CENTRAL PHARMACY] | 1 | Legacy NDC, 1 package rows | 20190118_2e9928cb-0105-4552-9d41-260de8934a64.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 |
|---|
| 53808-1109-1 | 53808110901 | 30 TABLET in 1 BLISTER PACK (53808-1109-1) | 30 tablet | 2018-04-25 | 0000-00-00 | No | No | Current |