Ocuvel (Adler-Stern Pharmaceuticals, LLC)
Welcome to the PulseAid listing for the Ocuvel drug offered from Adler-Stern Pharmaceuticals, LLC. This Copper [Chemical/Ingredient],Copper-containing Intrauterine Device [EPC],Decreased Embryonic Implantation [PE],Decreased Sperm Motility [PE],Inhibit Ovum Fertilization [PE] 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: | Adler-Stern Pharmaceuticals, LLC |
NON-PROPRIETARY NAME: | Ocuvel |
SUBSTANCE NAME: | FOLIC ACID; ASCORBIC ACID; ALPHA-TOCOPHEROL ACETATE; ZINC OXIDE; COPPER; LUTEIN; ZEAXANTHIN |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | Copper [Chemical/Ingredient],Copper-containing Intrauterine Device [EPC],Decreased Embryonic Implantation [PE],Decreased Sperm Motility [PE],Inhibit Ovum Fertilization [PE] |
ROUTE: | ORAL |
DOSAGE FORM: | CAPSULE |
MARKETING CATEGORY NAME: | UNAPPROVED DRUG OTHER |
START MARKETING DATE: | 2014-11-05 |
END MARKETING DATE: | 0000-00-00 |
Ocuvel HUMAN PRESCRIPTION DRUG Details:
Item Description | Ocuvel from Adler-Stern Pharmaceuticals, LLC |
LABELER NAME: | Adler-Stern Pharmaceuticals, LLC |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 1; 500; 400; 80; 2; 10; 2(mg/1; mg/1; [iU]/1; mg/1; mg/1; mg/1; mg/1) |
START MARKETING DATE: | 2014-11-05 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 69054-210_41bc18d9-9498-41c4-b84e-5bb6d2d52543 |
PRODUCT NDC: | 69054-210 |
APPLICATION NUMBER: | |
Other FOLIC ACID; ASCORBIC ACID; ALPHA-TOCOPHEROL ACETATE; ZINC OXIDE; COPPER; LUTEIN; ZEAXANTHIN Pharmaceutical Manufacturers / Labelers: