Furosemide
- Product NDC
- 10135-834
- 11-digit product format
- 101350834
- Labeler code
- 10135
- Product ID
- 10135-834_4bd1ae61-8ab9-342a-e063-6394a90af1d2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- FUROSEMIDE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Marlex Pharmaceuticals, Inc.
- Application
- NDA018569
- Marketing category
- NDA
- Marketing start
- 2026-03-01
- Substance
- FUROSEMIDE
- Active strength
- 80 mg/1
- Pharmacologic classes
- Increased Diuresis at Loop of Henle [PE], Loop Diuretic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- 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 |
|---|
| 10135-834-01 | 10135083401 | 100 TABLET in 1 BOTTLE (10135-834-01) | 100 tablet | 2026-03-01 | No | No | Historical |
| 10135-834-05 | 10135083405 | 500 TABLET in 1 BOTTLE (10135-834-05) | 500 tablet | 2026-03-01 | No | No | Historical |
| 10135-834-90 | 10135083490 | 90 TABLET in 1 BOTTLE (10135-834-90) | 90 tablet | 2026-03-01 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Furosemide Tablets, USP | Marlex Pharmaceuticals, Inc. | 2026-03-01 | HUMAN PRESCRIPTION DRUG LABEL | 1 |