Furosemide
- Product NDC
- 0615-1569
- 11-digit product format
- 006151569
- Labeler code
- 0615
- Product ID
- 0615-1569_7c5111c8-7a8c-4e90-b257-4379b7d469de
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Furosemide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NCS HealthCare of KY, Inc dba Vangard Labs
- Application
- NDA018413
- Marketing category
- NDA
- Marketing start
- 1983-11-30
- 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
FDA-Initiated Inactive NDC Indexing#