Furosemide
- Product NDC
- 71610-635
- 11-digit product format
- 716100635
- Labeler code
- 71610
- Product ID
- 71610-635_e9231c86-1596-42eb-b1f8-61747c75f030
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- furosemide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Aphena Pharma Solutions - Tennessee, LLC
- Application
- ANDA076796
- Marketing category
- ANDA
- Marketing start
- 2022-01-04
- 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 |
|---|
| 71610-635-30 | 71610063530 | 30 TABLET in 1 BOTTLE (71610-635-30) | 30 tablet | 2022-02-22 | No | No | Historical |
| 71610-635-45 | 71610063545 | 45 TABLET in 1 BOTTLE (71610-635-45) | 45 tablet | 2022-03-08 | No | No | Historical |
| 71610-635-53 | 71610063553 | 60 TABLET in 1 BOTTLE (71610-635-53) | 60 tablet | 2022-02-22 | No | No | Historical |
| 71610-635-60 | 71610063560 | 90 TABLET in 1 BOTTLE (71610-635-60) | 90 tablet | 2022-02-22 | No | No | Historical |
| 71610-635-80 | 71610063580 | 180 TABLET in 1 BOTTLE (71610-635-80) | 180 tablet | 2022-02-22 | No | No | Historical |
| 71610-635-92 | 71610063592 | 270 TABLET in 1 BOTTLE (71610-635-92) | 270 tablet | 2022-02-22 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| FUROSEMIDE TABLETS, USP | Aphena Pharma Solutions - Tennessee, LLC | 2022-03-10 | HUMAN PRESCRIPTION DRUG LABEL | 2 |