Spironolactone
- Product NDC
- 0615-8221
- 11-digit product format
- 006158221
- Labeler code
- 0615
- Product ID
- 0615-8221_8e86ae64-a22b-4f6d-bb04-0175809a86ba
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- spironolactone
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- NCS HealthCare of KY, Inc dba Vangard Labs
- Application
- ANDA203512
- Marketing category
- ANDA
- Marketing start
- 2018-09-10
- 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
- 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 |
|---|
| 0615-8221-39 | 00615822139 | 30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8221-39) | 2018-09-10 | 0000-00-00 | No | No | Current |