Furosemide
- Product NDC
- 67296-0650
- 11-digit product format
- 672960650
- Labeler code
- 67296
- Product ID
- 67296-0650_73b6c4d0-18f6-4a87-b0f4-14a502f6f98c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Furosemide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- RedPharm Drug Inc.
- Application
- ANDA078010
- Marketing category
- ANDA
- Marketing start
- 2009-01-29
- 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 |
|---|
| 67296-0650-1 | Furosemide | 15 in 1 BOTTLE | TABLET | 15 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 67296-0650 | FUROSEMIDE TABLET [REDPHARM DRUG INC.] | 1 | Legacy NDC, 1 package rows | 20110726_708b157c-845d-4776-9ced-6ae4aae10210.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 67296-0650-1 | 67296065001 | 15 in 1 BOTTLE | Historical |