Osteodoron PM Bone Support (Uriel Pharmacy Inc)


Welcome to the PulseAid listing for the Osteodoron PM Bone Support drug offered from Uriel Pharmacy 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: Uriel Pharmacy Inc
NON-PROPRIETARY NAME: OYSTER SHELL CALCIUM CARBONATE, CRUDE WHITE OAK BARK CALCIUM FLUORIDE SILICON DIOXIDE
SUBSTANCE NAME: OYSTER SHELL CALCIUM CARBONATE, CRUDE; WHITE OAK BARK; CALCIUM FLUORIDE; SILICON DIOXIDE
TYPE: HUMAN OTC DRUG
PHARMA CLASS:
ROUTE: ORAL
DOSAGE FORM: POWDER
MARKETING CATEGORY NAME: UNAPPROVED HOMEOPATHIC
START MARKETING DATE: 2009-09-01
END MARKETING DATE: 0000-00-00


Osteodoron PM Bone Support HUMAN OTC DRUG Details:

Item DescriptionOsteodoron PM Bone Support from Uriel Pharmacy Inc
LABELER NAME: Uriel Pharmacy Inc
DEA SCHEDULE:
ACTIVE STRENGTH: 1; 4; 6; 6([hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1)
START MARKETING DATE: 2009-09-01
END MARKETING DATE: 0000-00-00
PRODUCT ID: 48951-7097_ff723fd0-2df1-11df-8a39-0800200c9a66
PRODUCT NDC: 48951-7097
APPLICATION NUMBER:

Other OYSTER SHELL CALCIUM CARBONATE, CRUDE; WHITE OAK BARK; CALCIUM FLUORIDE; SILICON DIOXIDE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Uriel Pharmacy IncOsteodoron PM Bone Support