Spironolactone
- Product NDC
- 72162-2150
- 11-digit product format
- 721622150
- Labeler code
- 72162
- Product ID
- 72162-2150_72d2084e-af77-4da8-a5c9-60e32a2677cc
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- spironolactone
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA040424
- Marketing category
- ANDA
- Marketing start
- 1981-02-03
- Substance
- SPIRONOLACTONE
- Active strength
- 25 mg/1
- Pharmacologic classes
- Aldosterone Antagonist [EPC], Aldosterone Antagonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- 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 |
|---|
| 72162-2150-5 | 72162215005 | 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72162-2150-5) | 1981-02-03 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Spironolactone | Bryant Ranch Prepack | 2026-03-20 | HUMAN PRESCRIPTION DRUG LABEL | 101 |