Spironolactone
- Product NDC
- 16714-638
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- spironolactone
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- NorthStar RxLLC
- Application
- ANDA203512
- Marketing category
- ANDA
- Substance
- SPIRONOLACTONE
- Current FDA listing
- Historical FDA.report record
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 16714-638-01 | 100 TABLET, FILM COATED in 1 BOTTLE (16714-638-01) | 2017-06-02 | 0000-00-00 | No | Current |
| 16714-638-02 | 500 TABLET, FILM COATED in 1 BOTTLE (16714-638-02) | 2017-06-02 | 0000-00-00 | No | Current |