Spironolactone
- Product NDC
- 43353-239
- 11-digit product format
- 433530239
- Labeler code
- 43353
- Product ID
- 43353-239_8d235883-ec5d-4a18-8f39-e69b0965e032
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- spironolactone
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Aphena Pharma Solutions - Tennessee, LLC
- Application
- ANDA040750
- Marketing category
- ANDA
- Marketing start
- 2006-08-29
- Marketing end
- 2021-07-31
- Substance
- SPIRONOLACTONE
- Active strength
- 25 mg/1
- Pharmacologic classes
- Aldosterone Antagonist [EPC],Aldosterone Antagonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 43353-239-60 | 43353023960 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43353-239-60) | 2018-08-29 | 2021-07-31 | No | No | Current |