LEVONORGESTREL AND ETHINYL ESTRADIOL
- Product NDC
- 70700-104
- 11-digit product format
- 707000104
- Labeler code
- 70700
- Product ID
- 70700-104_9a54dd0b-87e6-0d7f-d8bf-78ecd23f8e12
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Levonorgestrel and Ethinyl Estradiol Tablets
- Dosage form
- KIT
- Labeler
- Xiromed, LLC.
- Application
- ANDA202507
- Marketing category
- ANDA
- Marketing start
- 2017-08-08
- Marketing end
- 0000-00-00
- Active strength
- 0
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record