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 Description | Thyrolar from Forest Laboratories, Inc |
LABELER NAME: | Forest Laboratories, Inc |
DEA SCHEDULE: |
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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: