NORETHINDRONE ACETATE AND ETHINYL ESTRADIOL
- Product NDC
- 50090-3395
- 11-digit product format
- 500903395
- Labeler code
- 50090
- Product ID
- 50090-3395_9000891d-b199-4d51-81ad-cb5f217bda51
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- norethindrone acetate and ethinyl estradiol
- Dosage form
- KIT
- Labeler
- A-S Medication Solutions
- Application
- ANDA202772
- Marketing category
- ANDA
- Marketing start
- 2014-07-16
- 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