Osteopar (Energique, Inc.)


Welcome to the PulseAid listing for the Osteopar drug offered from Energique, 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: Energique, Inc.
NON-PROPRIETARY NAME: Equisetum Hyemale, Symphytum Officinale, Calcarea Carbonica, Calcarea Fluorica, Calcarea Phosphorica, Medulla Ossis Suis, Ossa Sepia, Silicea, Hekla Lava
SUBSTANCE NAME: EQUISETUM HYEMALE; COMFREY ROOT; OYSTER SHELL CALCIUM CARBONATE, CRUDE; CALCIUM FLUORIDE; TRIBASIC CALCIUM PHOSPHATE; SUS SCROFA BONE MARROW; SEPIA ESCULENTA BONE; SILICON DIOXIDE; HEKLA LAVA
TYPE: HUMAN OTC DRUG
PHARMA CLASS:
ROUTE: ORAL
DOSAGE FORM: LIQUID
MARKETING CATEGORY NAME: UNAPPROVED HOMEOPATHIC
START MARKETING DATE: 2016-06-16
END MARKETING DATE: 0000-00-00


Osteopar HUMAN OTC DRUG Details:

Item DescriptionOsteopar from Energique, Inc.
LABELER NAME: Energique, Inc.
DEA SCHEDULE:
ACTIVE STRENGTH: 3; 6; 12; 12; 12; 12; 12; 12; 15([hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL)
START MARKETING DATE: 2016-06-16
END MARKETING DATE: 0000-00-00
PRODUCT ID: 44911-0367_f6fa00bc-c95a-4c1e-be28-51596842b112
PRODUCT NDC: 44911-0367
APPLICATION NUMBER:

Other EQUISETUM HYEMALE; COMFREY ROOT; OYSTER SHELL CALCIUM CARBONATE, CRUDE; CALCIUM FLUORIDE; TRIBASIC CALCIUM PHOSPHATE; SUS SCROFA BONE MARROW; SEPIA ESCULENTA BONE; SILICON DIOXIDE; HEKLA LAVA Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Energique, Inc.Osteopar