Foltrate (Poly Pharmaceuticals, Inc.)


Welcome to the PulseAid listing for the Foltrate drug offered from Poly Pharmaceuticals, Inc.. This pharmaceutical is classified as a HUMAN OTC 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 OTC DRUG drug type category.
LABELER NAME / MANUFACTURER: Poly Pharmaceuticals, Inc.
NON-PROPRIETARY NAME: Folic Acid and Cyanocobalamin
SUBSTANCE NAME: FOLIC ACID; CYANOCOBALAMIN
TYPE: HUMAN OTC DRUG
PHARMA CLASS:
ROUTE: ORAL
DOSAGE FORM: TABLET, FILM COATED
MARKETING CATEGORY NAME: UNAPPROVED DRUG OTHER
START MARKETING DATE: 2010-08-26
END MARKETING DATE: 0000-00-00


Foltrate HUMAN OTC DRUG Details:

Item DescriptionFoltrate from Poly Pharmaceuticals, Inc.
LABELER NAME: Poly Pharmaceuticals, Inc.
DEA SCHEDULE:
ACTIVE STRENGTH: 1; 500(mg/1; ug/1)
START MARKETING DATE: 2010-08-26
END MARKETING DATE: 0000-00-00
PRODUCT ID: 50991-323_6ba903a8-6be6-4bef-9f77-f3cf6fa38d44
PRODUCT NDC: 50991-323
APPLICATION NUMBER:

Other FOLIC ACID; CYANOCOBALAMIN Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Poly Pharmaceuticals, Inc.Foltrate