Forteo (Eli Lilly and Company)


Welcome to the PulseAid listing for the Forteo drug offered from Eli Lilly and Company. This Parathyroid Hormone [Chemical/Ingredient],Parathyroid Hormone Analog [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: Eli Lilly and Company
NON-PROPRIETARY NAME: Teriparatide
SUBSTANCE NAME: TERIPARATIDE
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: Parathyroid Hormone [Chemical/Ingredient],Parathyroid Hormone Analog [EPC]
ROUTE: SUBCUTANEOUS
DOSAGE FORM: INJECTION, SOLUTION
MARKETING CATEGORY NAME: NDA
START MARKETING DATE: 2002-11-26
END MARKETING DATE: 0000-00-00


Forteo HUMAN PRESCRIPTION DRUG Details:

Item DescriptionForteo from Eli Lilly and Company
LABELER NAME: Eli Lilly and Company
DEA SCHEDULE:
ACTIVE STRENGTH: 250(ug/mL)
START MARKETING DATE: 2002-11-26
END MARKETING DATE: 0000-00-00
PRODUCT ID: 0002-8400_4d0a0023-d348-41dd-a689-43971e41d26f
PRODUCT NDC: 0002-8400
APPLICATION NUMBER: NDA021318

Other TERIPARATIDE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Eli Lilly and CompanyForteo