Spironolactone
- Product NDC
- 63629-8132
- 11-digit product format
- 636298132
- Labeler code
- 63629
- Product ID
- 63629-8132_8f286d6d-0bf6-4d99-a83e-7c5db9fb374f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- spironolactone
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA203512
- Marketing category
- ANDA
- Marketing start
- 2017-06-02
- Marketing end
- 0000-00-00
- Substance
- SPIRONOLACTONE
- Active strength
- 100 mg/1
- Pharmacologic classes
- Aldosterone Antagonist [EPC],Aldosterone Antagonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 63629-8132-1 | 63629813201 | 30 TABLET, FILM COATED in 1 BOTTLE (63629-8132-1) | 2019-07-29 | 0000-00-00 | No | No | Current |