AUBRA (Afaxys Pharma, LLC)
Welcome to the PulseAid listing for the AUBRA drug offered from Afaxys Pharma, LLC. This pharmaceutical is classified as a HUMAN PRESCRIPTION DRUG. Below, you can view details for this drug, such as its dosage form, route of delivery, start market/end market dates, and more. We have also randomly listed additional pharmaceuticals used in the same HUMAN PRESCRIPTION DRUG drug type category.
LABELER NAME / MANUFACTURER: | Afaxys Pharma, LLC |
NON-PROPRIETARY NAME: | Levonorgestrel and Ethinyl Estradiol |
SUBSTANCE NAME: | |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | |
ROUTE: | |
DOSAGE FORM: | KIT |
MARKETING CATEGORY NAME: | ANDA |
START MARKETING DATE: | 2013-10-15 |
END MARKETING DATE: | 0000-00-00 |
AUBRA HUMAN PRESCRIPTION DRUG Details:
Item Description | AUBRA from Afaxys Pharma, LLC |
LABELER NAME: | Afaxys Pharma, LLC |
DEA SCHEDULE: | |
ACTIVE STRENGTH: | () |
START MARKETING DATE: | 2013-10-15 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 50102-120_d301a49d-1dc6-47da-acd4-ba6a3364794b |
PRODUCT NDC: | 50102-120 |
APPLICATION NUMBER: | ANDA200245 |