Furosemide
- Product NDC
- 58118-0143
- 11-digit product format
- 581180143
- Labeler code
- 58118
- Product ID
- 58118-0143_b025bbc6-d32a-48b6-e053-2995a90a0c00
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Furosemide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Clinical Solutions Wholesale, LLC
- 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
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 58118-0143 | FUROSEMIDE TABLET [CLINICAL SOLUTIONS WHOLESALE, LLC] | 7 | Legacy NDC | 20200926_44b7e645-cfcd-4915-bb8e-7be3bff7e4ba.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 58118-0143-8 | 58118014308 | 30 TABLET in 1 BLISTER PACK (58118-0143-8) | 30 tablet | 2016-10-18 | 0000-00-00 | No | No | Current |