Junel Fe 1.5/30 (Barr Laboratories Inc.)
Welcome to the PulseAid listing for the Junel Fe 1.5/30 drug offered from Barr Laboratories Inc.. 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: | Barr Laboratories Inc. |
NON-PROPRIETARY NAME: | norethindrone acetate and ethinyl estradiol, and ferrous fumarate |
SUBSTANCE NAME: | |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | |
ROUTE: | |
DOSAGE FORM: | KIT |
MARKETING CATEGORY NAME: | ANDA |
START MARKETING DATE: | 2003-09-18 |
END MARKETING DATE: | 0000-00-00 |
Junel Fe 1.5/30 HUMAN PRESCRIPTION DRUG Details:
Item Description | Junel Fe 1.5/30 from Barr Laboratories Inc. |
LABELER NAME: | Barr Laboratories Inc. |
DEA SCHEDULE: | |
ACTIVE STRENGTH: | () |
START MARKETING DATE: | 2003-09-18 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 0555-9028_ceddd4c3-4827-4294-8767-d1e781a1d611 |
PRODUCT NDC: | 0555-9028 |
APPLICATION NUMBER: | ANDA076064 |