Furosemide
- Product NDC
- 68071-4349
- 11-digit product format
- 680714349
- Labeler code
- 68071
- Product ID
- 68071-4349_bb7b9180-6386-9de0-e053-2a95a90a4186
- 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#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-4349-1 | 68071434901 | 10 TABLET in 1 BOTTLE (68071-4349-1) | 10 tablet | 2018-03-22 | 0000-00-00 | No | No | Current |
| 68071-4349-3 | 68071434903 | 30 TABLET in 1 BOTTLE (68071-4349-3) | 30 tablet | 2018-03-22 | 0000-00-00 | No | No | Current |
| 68071-4349-6 | 68071434906 | 60 TABLET in 1 BOTTLE (68071-4349-6) | 60 tablet | 2018-03-22 | 0000-00-00 | No | No | Current |
| 68071-4349-8 | 68071434908 | 180 TABLET in 1 BOTTLE (68071-4349-8) | 180 tablet | 2018-03-22 | 0000-00-00 | No | No | Current |
| 68071-4349-9 | 68071434909 | 90 TABLET in 1 BOTTLE (68071-4349-9) | 90 tablet | 2018-03-22 | 0000-00-00 | No | No | Current |