Spironolactone
- Product NDC
- 50436-5015
- 11-digit product format
- 504365015
- Labeler code
- 50436
- Product ID
- 50436-5015_be118d7d-fa6c-44e5-9420-9a824d59ac22
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- spironolactone
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Unit Dose Services
- Application
- ANDA089424
- Marketing category
- ANDA
- Marketing start
- 1986-07-23
- Marketing end
- 0000-00-00
- Substance
- SPIRONOLACTONE
- Active strength
- 100 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