spironolactone
- Product NDC
- 55700-934
- 11-digit product format
- 557000934
- Labeler code
- 55700
- Product ID
- 55700-934_98f29b40-debc-42be-a6e0-f48c5c4021bf
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- spironolactone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Quality Care Products, LLC
- Application
- ANDA205936
- Marketing category
- ANDA
- Marketing start
- 2021-09-01
- Marketing end
- 0000-00-00
- Substance
- SPIRONOLACTONE
- Active strength
- 50 mg/1
- Pharmacologic classes
- Aldosterone Antagonist [EPC],Aldosterone Antagonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55700-934-30 | 55700093430 | 30 TABLET in 1 BOTTLE (55700-934-30) | 30 tablet | 2021-09-01 | 0000-00-00 | No | No | Current |