Furosemide
- Product NDC
- 63187-739
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Furosemide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA077293
- Marketing category
- ANDA
- Substance
- FUROSEMIDE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 63187-739-10 | 10 TABLET in 1 BOTTLE (63187-739-10) | 2017-03-01 | | No | Historical |
| 63187-739-30 | 30 TABLET in 1 BOTTLE (63187-739-30) | 2016-10-03 | | No | Historical |
| 63187-739-60 | 60 TABLET in 1 BOTTLE (63187-739-60) | 2016-10-03 | | No | Historical |
| 63187-739-90 | 90 TABLET in 1 BOTTLE (63187-739-90) | 2016-10-03 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| FUROSEMIDE TABLETS, USP | Proficient Rx LP | 2022-12-01 | HUMAN PRESCRIPTION DRUG LABEL | 6 |