Spironolactone
- Product NDC
- 55700-968
- 11-digit product format
- 557000968
- Labeler code
- 55700
- Product ID
- 55700-968_b9f15e01-5d03-49d3-ae1e-e0cb899a2cb6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- spironolactone
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Quality Care Products, LLC
- Application
- ANDA203512
- Marketing category
- ANDA
- Marketing start
- 2022-07-13
- 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
- 2023-12-31
- 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 |
|---|
| 55700-968-30 | 55700096830 | 30 TABLET, FILM COATED in 1 BOTTLE (55700-968-30) | 2022-07-13 | 0000-00-00 | No | No | Current |