Furosemide
- Product NDC
- 50090-5702
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Furosemide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA077293
- Marketing category
- ANDA
- Substance
- FUROSEMIDE
- Current FDA listing
- Yes
Related Records
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|---|---|---|---|---|
| 50090-5702-0 | 100 TABLET in 1 BOTTLE (50090-5702-0) | 2021-09-23 | No | Historical | |
| 50090-5702-1 | 180 TABLET in 1 BOTTLE (50090-5702-1) | 2023-04-18 | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|---|---|---|---|
| FUROSEMIDE TABLETS, USP 20 mg, 40 mg and 80 mg | A-S Medication Solutions | 2023-04-19 | HUMAN PRESCRIPTION DRUG LABEL | 5 |