Furosemide
- Product NDC
- 63187-517
- 11-digit product format
- 631870517
- Labeler code
- 63187
- Product ID
- 63187-517_2a96ac85-a5c3-48f0-8ab9-7c57ff793502
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Furosemide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA077293
- Marketing category
- ANDA
- Marketing start
- 2006-02-01
- 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
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 7LXU5N7ZO5 | FUROSEMIDE | 54-31-9 | FUROSEMIDE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 63187-517-30 | 63187051730 | 30 TABLET in 1 BOTTLE (63187-517-30) | 30 tablet | 2018-12-01 | No | No | Historical |
| 63187-517-60 | 63187051760 | 60 TABLET in 1 BOTTLE (63187-517-60) | 60 tablet | 2018-12-01 | No | No | Historical |
| 63187-517-90 | 63187051790 | 90 TABLET in 1 BOTTLE (63187-517-90) | 90 tablet | 2018-12-01 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Furosemide Tablets, USP | Proficient Rx LP | 2021-01-01 | HUMAN PRESCRIPTION DRUG LABEL | 4 |