Thyrolar (Forest Laboratories, Inc)


Welcome to the PulseAid listing for the Thyrolar drug offered from Forest Laboratories, Inc. This l-Triiodothyronine [EPC],Triiodothyronine [Chemical/Ingredient],l-Thyroxine [EPC],Thyroxine [Chemical/Ingredient] 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: Forest Laboratories, Inc
NON-PROPRIETARY NAME: liothyronine sodium, LEVOTHYROXINE SODIUM
SUBSTANCE NAME: LIOTHYRONINE SODIUM; LEVOTHYROXINE SODIUM
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: l-Triiodothyronine [EPC],Triiodothyronine [Chemical/Ingredient],l-Thyroxine [EPC],Thyroxine [Chemical/Ingredient]
ROUTE: ORAL
DOSAGE FORM: TABLET
MARKETING CATEGORY NAME: NDA
START MARKETING DATE: 1969-11-21
END MARKETING DATE: 0000-00-00


Thyrolar HUMAN PRESCRIPTION DRUG Details:

Item DescriptionThyrolar from Forest Laboratories, Inc
LABELER NAME: Forest Laboratories, Inc
DEA SCHEDULE:
ACTIVE STRENGTH: 3.1; 12.5(ug/1; ug/1)
START MARKETING DATE: 1969-11-21
END MARKETING DATE: 0000-00-00
PRODUCT ID: 0456-0040_a87635bc-a599-42e1-b776-92207c225b0a
PRODUCT NDC: 0456-0040
APPLICATION NUMBER: NDA016807

Other LIOTHYRONINE SODIUM; LEVOTHYROXINE SODIUM Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Forest Laboratories, IncThyrolar