Furosemide
- Product NDC
- 64125-116
- 11-digit product format
- 641250116
- Labeler code
- 64125
- Product ID
- 64125-116_cd25b50f-e1c5-4ed0-a370-e3b8a7b77f01
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Furosemide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Excellium Pharmaceutical Inc.
- Application
- ANDA077293
- Marketing category
- ANDA
- Marketing start
- 2006-02-01
- Marketing end
- 0000-00-00
- Substance
- FUROSEMIDE
- Active strength
- 20 mg/1
- Pharmacologic classes
- Increased Diuresis at Loop of Henle [PE],Loop Diuretic [EPC]
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- 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 |
|---|
| 64125-116-01 | Furosemide | 100 in 1 BOTTLE | TABLET | 100 | | 1 |
| 64125-116-10 | Furosemide | 1000 in 1 BOTTLE | TABLET | 1000 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 64125-116 | FUROSEMIDE (FUROSEMIDE) TABLET [EXCELLIUM PHARMACEUTICAL INC.] | 1 | Legacy NDC, 2 package rows | 20120831_79d9aef8-cfb9-4f6e-ac15-f830d7ea2324.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 64125-116-01 | 64125011601 | 100 in 1 BOTTLE | Historical |
| 64125-116-10 | 64125011610 | 1000 in 1 BOTTLE | Historical |