spironolactone
- Product NDC
- 59762-5011
- 11-digit product format
- 597625011
- Labeler code
- 59762
- Product ID
- 59762-5011_82d1b2a5-4b7d-4d49-a0d3-4001cd6e1bb7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- spironolactone
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Greenstone LLC
- Application
- NDA012151
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 1960-01-21
- Marketing end
- 2021-03-31
- 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 |
|---|
| 59762-5011-2 | 59762501102 | 500 TABLET, FILM COATED in 1 BOTTLE (59762-5011-2) | 1960-01-21 | 2021-03-31 | No | No | Current |