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 DescriptionOcuvel from Adler-Stern Pharmaceuticals, LLC
LABELER NAME: Adler-Stern Pharmaceuticals, LLC
DEA SCHEDULE:
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:

Manufacturer / LabelerProprietary Name
Adler-Stern Pharmaceuticals, LLCOcuvel