Furosemide
- Product NDC
- 71610-309
- 11-digit product format
- 716100309
- Labeler code
- 71610
- Product ID
- 71610-309_f0960a17-009b-4da4-b2cc-7851e22a2165
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Furosemide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Aphena Pharma Solutions - Tennessee, LLC
- Application
- NDA018823
- Marketing category
- NDA
- Marketing start
- 1983-11-10
- Marketing end
- 0000-00-00
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
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 | Marketing end | Sample | Exclude flag | Status |
|---|
| 71610-309-30 | 71610030930 | 30 TABLET in 1 BOTTLE, PLASTIC (71610-309-30) | 30 tablet | 2019-07-17 | 0000-00-00 | No | No | Current |
| 71610-309-45 | 71610030945 | 45 TABLET in 1 BOTTLE, PLASTIC (71610-309-45) | 45 tablet | 2019-07-17 | 0000-00-00 | No | No | Current |
| 71610-309-53 | 71610030953 | 60 TABLET in 1 BOTTLE, PLASTIC (71610-309-53) | 60 tablet | 2019-07-17 | 0000-00-00 | No | No | Current |
| 71610-309-60 | 71610030960 | 90 TABLET in 1 BOTTLE, PLASTIC (71610-309-60) | 90 tablet | 2019-07-17 | 0000-00-00 | No | No | Current |
| 71610-309-80 | 71610030980 | 180 TABLET in 1 BOTTLE, PLASTIC (71610-309-80) | 180 tablet | 2019-07-17 | 0000-00-00 | No | No | Current |
| 71610-309-92 | 71610030992 | 270 TABLET in 1 BOTTLE, PLASTIC (71610-309-92) | 270 tablet | 2019-07-17 | 0000-00-00 | No | No | Current |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| FUROSEMIDE Tablets USP | Aphena Pharma Solutions - Tennessee, LLC | 2019-07-17 | HUMAN PRESCRIPTION DRUG LABEL | 1 |