MaxFe (Pronova Corporation)


Welcome to the PulseAid listing for the MaxFe drug offered from Pronova Corporation. This Vitamin B 12 [Chemical/Ingredient],Vitamin B12 [EPC] 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: Pronova Corporation
NON-PROPRIETARY NAME: ascorbic acid, folic acid, vitamin b-12, biotin, iron, magnesium, zinc
SUBSTANCE NAME: ASCORBIC ACID; FOLIC ACID; CYANOCOBALAMIN; BIOTIN; IRON; MAGNESIUM; ZINC; DOCUSATE SODIUM
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: Vitamin B 12 [Chemical/Ingredient],Vitamin B12 [EPC]
ROUTE: ORAL
DOSAGE FORM: TABLET
MARKETING CATEGORY NAME: UNAPPROVED DRUG OTHER
START MARKETING DATE: 2014-06-01
END MARKETING DATE: 0000-00-00


MaxFe HUMAN PRESCRIPTION DRUG Details:

Item DescriptionMaxFe from Pronova Corporation
LABELER NAME: Pronova Corporation
DEA SCHEDULE:
ACTIVE STRENGTH: 100; 1; 60; 150; 160; 6.5; 12; 50(mg/1; mg/1; ug/1; ug/1; mg/1; mg/1; mg/1; mg/1)
START MARKETING DATE: 2014-06-01
END MARKETING DATE: 0000-00-00
PRODUCT ID: 67555-140_a769b672-5a74-4d2a-a01a-e7c3c124d94e
PRODUCT NDC: 67555-140
APPLICATION NUMBER:

Other ASCORBIC ACID; FOLIC ACID; CYANOCOBALAMIN; BIOTIN; IRON; MAGNESIUM; ZINC; DOCUSATE SODIUM Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Pronova CorporationMaxFe