LEVONORGESTREL AND ETHINYL ESTRADIOL
- Product NDC
- 50090-2534
- 11-digit product format
- 500902534
- Labeler code
- 50090
- Product ID
- 50090-2534_4ed7c1ab-e0f0-42fc-b86d-399f26c0575f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Levonorgestrel and Ethinyl Estradiol
- Dosage form
- KIT
- Labeler
- A-S Medication Solutions
- Application
- ANDA200245
- Marketing category
- ANDA
- Marketing start
- 2014-06-26
- Marketing end
- 0000-00-00
- Active strength
- 0
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record