Furosemide
- Product NDC
- 68071-3536
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Furosemide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA216629
- Marketing category
- ANDA
- Substance
- FUROSEMIDE
- Current FDA listing
- Yes
Related Records
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|---|---|---|---|---|
| 68071-3536-3 | 30 TABLET in 1 BOTTLE (68071-3536-3) | 2023-11-28 | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|---|---|---|---|
| Furosemide Tablets, USP 20 mg, 40 mg, and 80 mg Rx Only | NuCare Pharmaceuticals,Inc. | 2025-02-03 | HUMAN PRESCRIPTION DRUG LABEL | 2 |