Spironolactone
- Product NDC
- 60760-771
- 11-digit product format
- 607600771
- Labeler code
- 60760
- Product ID
- 60760-771_7b069009-00e1-10c2-e053-2991aa0aca3b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- spironolactone
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- St. Mary's Medical Park Pharmacy
- Application
- ANDA203512
- Marketing category
- ANDA
- Marketing start
- 2018-09-27
- 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 |
|---|
| 60760-771-90 | 60760077190 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-771-90) | 2018-09-27 | 0000-00-00 | No | No | Current |