Levonorgestrel and Ethinyl Estradiol
- Product NDC
- 57297-857
- 11-digit product format
- 572970857
- Labeler code
- 57297
- Product ID
- 57297-857_9c0503d4-6400-4daa-8fc9-0665324c599b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Levonorgestrel and Ethinyl Estradiol
- Dosage form
- KIT
- Labeler
- LUPIN LIMITED
- Application
- ANDA200248
- Marketing category
- ANDA
- Marketing start
- 2015-12-03
- 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#