Furosemide
- Product NDC
- 68071-2461
- 11-digit product format
- 680712461
- Labeler code
- 68071
- Product ID
- 68071-2461_c5d9a09f-df6f-50a1-e053-2995a90abd36
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- furosemide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA076796
- Marketing category
- ANDA
- Marketing start
- 2004-03-26
- 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
FDA-Initiated Inactive NDC Indexing#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68071-2461 | FUROSEMIDE TABLET [NUCARE PHARMACEUTICALS,INC.] | 1 | Legacy NDC | 20210629_c5d9a09f-df6e-50a1-e053-2995a90abd36.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-2461-1 | 68071246101 | 100 TABLET in 1 BOTTLE, PLASTIC (68071-2461-1) | 100 tablet | 2021-06-28 | 0000-00-00 | No | No | Current |