Spironolactone
- Product NDC
- 72189-495
- 11-digit product format
- 721890495
- Labeler code
- 72189
- Product ID
- 72189-495_2c4e3760-8448-4adb-e063-6394a90a5ffc
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Spironolactone
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- Direct_Rx
- Application
- ANDA040750
- Marketing category
- ANDA
- Marketing start
- 2023-07-05
- Substance
- SPIRONOLACTONE
- Active strength
- 100 mg/1
- Pharmacologic classes
- Aldosterone Antagonist [EPC], Aldosterone Antagonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
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 | Sample | Exclude flag | Status |
|---|
| 72189-495-90 | 72189049590 | 90 TABLET, COATED in 1 BOTTLE (72189-495-90) | 2023-07-05 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Spironolactone | Direct_Rx | 2025-01-22 | HUMAN PRESCRIPTION DRUG LABEL | 2 |