Spironolactone
- Product NDC
- 50090-2728
- 11-digit product format
- 500902728
- Labeler code
- 50090
- Product ID
- 50090-2728_8f33f6bd-c039-4c70-9ec9-c6989a17e6d8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- spironolactone
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA203253
- Marketing category
- ANDA
- Marketing start
- 2013-02-01
- 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
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 27O7W4T232 | SPIRONOLACTONE | 52-01-7 | SPIRONOLACTONE |