Spironolactone
- Product NDC
- 63187-634
- 11-digit product format
- 631870634
- Labeler code
- 63187
- Product ID
- 63187-634_e20358fa-96f3-4f29-92eb-3323969d7f4e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- spironolactone
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA040750
- Marketing category
- ANDA
- Marketing start
- 2006-08-29
- 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63187-634-30 | 63187063430 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (63187-634-30) | 2016-05-02 | 0000-00-00 | No | No | Current |
| 63187-634-60 | 63187063460 | 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (63187-634-60) | 2016-05-02 | 0000-00-00 | No | No | Current |
| 63187-634-90 | 63187063490 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (63187-634-90) | 2016-05-02 | 0000-00-00 | No | No | Current |