Furosemide
- Product NDC
- 67296-0691
- 11-digit product format
- 672960691
- Labeler code
- 67296
- Product ID
- 67296-0691_b8d06251-af5d-56a7-e053-2995a90a96fa
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- furosemide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- RedPharm Drug, Inc.
- Application
- NDA018487
- Marketing category
- NDA
- Marketing start
- 1981-08-27
- 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
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 67296-0691-1 | Furosemide | 30 in 1 BOTTLE | TABLET | 30 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 67296-0691 | FUROSEMIDE TABLET [REDPHARM DRUG, INC.] | 3 | Legacy NDC, 1 package rows | 20210114_88524616-e6bc-62fb-e053-2995a90a8395.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 |
|---|
| 67296-0691-1 | 67296069101 | 30 TABLET in 1 BOTTLE (67296-0691-1) | 30 tablet | 2019-01-01 | 0000-00-00 | No | No | Current |