Spironolactone
- Product NDC
- 55154-5055
- 11-digit product format
- 551545055
- Labeler code
- 55154
- Product ID
- 55154-5055_9572e6f6-b46c-44a0-8027-5942b02d2f86
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- spironolactone
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Cardinal Health
- Application
- ANDA040424
- Marketing category
- ANDA
- Marketing start
- 2011-02-04
- Marketing end
- 2020-01-31
- Substance
- SPIRONOLACTONE
- Active strength
- 100 mg/1
- Pharmacologic classes
- Aldosterone Antagonist [EPC],Aldosterone Antagonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 27O7W4T232 | SPIRONOLACTONE | 52-01-7 | SPIRONOLACTONE |