Spironolactone
- Product NDC
- 63629-2436
- 11-digit product format
- 636292436
- Labeler code
- 63629
- Product ID
- 63629-2436_b6eeaf89-fbc1-4458-a813-bd35b186e87b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- spironolactone
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA203253
- Marketing category
- ANDA
- Marketing start
- 2013-02-01
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 27O7W4T232 | SPIRONOLACTONE | 52-01-7 | SPIRONOLACTONE |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-2436-1 | 63629243601 | 100 TABLET, FILM COATED in 1 BOTTLE (63629-2436-1) | 2021-02-25 | 0000-00-00 | No | No | Current |