Furosemide
- Product NDC
- 17856-3755
- 11-digit product format
- 178563755
- Labeler code
- 17856
- Product ID
- 17856-3755_dbda651c-a981-4e87-a188-6594565504c2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Furosemide
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- Atlantic Biologicals Corps
- Application
- ANDA070433
- Marketing category
- ANDA
- Marketing start
- 1987-04-22
- Marketing end
- 0000-00-00
- Substance
- FUROSEMIDE
- Active strength
- 40 mg/5mL
- Pharmacologic classes
- Increased Diuresis at Loop of Henle [PE],Loop Diuretic [EPC]
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- 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 |
|---|
| 17856-3755-1 | Furosemide | 240 mL in 1 CUP | SOLUTION | 240 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 17856-3755 | FUROSEMIDE SOLUTION [ATLANTIC BIOLOGICALS CORPS] | 3 | Legacy NDC, 1 package rows | 20160504_4b4c2890-6434-488d-b5b4-00cba734b6e1.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 17856-3755-1 | 17856375501 | 240 mL in 1 CUP | 240 ml | Historical |