Furosemide
- Product NDC
- 68071-4022
- 11-digit product format
- 680714022
- Labeler code
- 68071
- Product ID
- 68071-4022_d59255ac-41ad-6da2-e053-2a95a90a09d2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Furosemide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA077293
- Marketing category
- ANDA
- Marketing start
- 2006-02-01
- Marketing end
- 0000-00-00
- Substance
- FUROSEMIDE
- Active strength
- 40 mg/1
- Pharmacologic classes
- Increased Diuresis at Loop of Henle [PE], Loop Diuretic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-4022-1 | 68071402201 | 100 TABLET in 1 BOTTLE (68071-4022-1) | 100 tablet | 2019-01-29 | 0000-00-00 | No | No | Current |