Spironolactone
- Product NDC
- 55700-587
- 11-digit product format
- 557000587
- Labeler code
- 55700
- Product ID
- 55700-587_3f8f36e0-44fd-4b56-a3e2-66fcf087eefe
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- spironolactone
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Lake Erie Medical DBA Quality Care Products LLC
- Application
- ANDA203253
- Marketing category
- ANDA
- Marketing start
- 2018-02-25
- Marketing end
- 0000-00-00
- Substance
- SPIRONOLACTONE
- Active strength
- 50 mg/1
- Pharmacologic classes
- Aldosterone Antagonist [EPC],Aldosterone Antagonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record