Levonorgestrel and Ethinyl Estradiol and Ethinyl Estradiol
- Product NDC
- 57297-848
- 11-digit product format
- 572970848
- Labeler code
- 57297
- Product ID
- 57297-848_f79de20e-4e48-4b93-b285-d7d388db1c62
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- levonorgestrel and ethinyl estradiol
- Dosage form
- KIT
- Labeler
- LUPIN LIMITED
- Application
- ANDA091674
- Marketing category
- ANDA
- Marketing start
- 2011-12-02
- Marketing end
- 0000-00-00
- Active strength
- 0
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#