Spironolactone
- Product NDC
- 71610-288
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- spironolactone
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Aphena Pharma Solutions - Tennessee, LLC
- Application
- ANDA203512
- Marketing category
- ANDA
- Substance
- SPIRONOLACTONE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 71610-288-30 | 30 TABLET, FILM COATED in 1 BOTTLE (71610-288-30) | 2019-05-31 | | No | Historical |
| 71610-288-45 | 45 TABLET, FILM COATED in 1 BOTTLE (71610-288-45) | 2019-05-31 | | No | Historical |
| 71610-288-60 | 90 TABLET, FILM COATED in 1 BOTTLE (71610-288-60) | 2019-05-31 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Spironolactone tablets, USP | Aphena Pharma Solutions - Tennessee, LLC | 2017-06-16 | HUMAN PRESCRIPTION DRUG LABEL | 1 |