spironolactone
- Product NDC
- 55700-713
- 11-digit product format
- 557000713
- Labeler code
- 55700
- Product ID
- 55700-713_915572e2-a1f8-406c-a4b1-c41afcda7732
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- spironolactone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Quality Care Products, LLC
- Application
- ANDA205936
- Marketing category
- ANDA
- Marketing start
- 2018-12-28
- Marketing end
- 0000-00-00
- Substance
- SPIRONOLACTONE
- Active strength
- 25 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55700-713-30 | 55700071330 | 30 TABLET in 1 BOTTLE (55700-713-30) | 30 tablet | 2018-12-28 | 0000-00-00 | No | No | Current |
| 55700-713-90 | 55700071390 | 90 TABLET in 1 BOTTLE (55700-713-90) | 90 tablet | 2019-06-14 | 0000-00-00 | No | No | Current |