Furosemide
- Product NDC
- 64725-0624
- 11-digit product format
- 647250624
- Labeler code
- 64725
- Product ID
- 64725-0624_031a2a0f-f357-45ed-9719-67ed4c7bca8f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Furosemide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- TYA Pharmaceuticals
- Application
- ANDA078010
- Marketing category
- ANDA
- Marketing start
- 2009-01-29
- 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
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record