Levonorgestrel and Ethinyl Estradiol
- Product NDC
- 57297-843
- 11-digit product format
- 572970843
- Labeler code
- 57297
- Product ID
- 57297-843_4f3cf691-0ecd-4399-9aff-7ac7173cf74c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Levonorgestrel and Ethinyl Estradiol
- Dosage form
- KIT
- Labeler
- LUPIN LIMITED
- Application
- ANDA091440
- Marketing category
- ANDA
- Marketing start
- 2012-10-24
- 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#