Durachol (Sterling Knight Pharmaceuticals,LLC)
Welcome to the PulseAid listing for the Durachol drug offered from Sterling Knight Pharmaceuticals,LLC. This Vitamin D [Chemical/Ingredient],Vitamin D [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: | Sterling Knight Pharmaceuticals,LLC |
NON-PROPRIETARY NAME: | Durachol |
SUBSTANCE NAME: | CHOLECALCIFEROL; FOLIC ACID |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | Vitamin D [Chemical/Ingredient],Vitamin D [EPC] |
ROUTE: | ORAL |
DOSAGE FORM: | CAPSULE |
MARKETING CATEGORY NAME: | UNAPPROVED DRUG OTHER |
START MARKETING DATE: | 2014-11-16 |
END MARKETING DATE: | 0000-00-00 |
Durachol HUMAN PRESCRIPTION DRUG Details:
Item Description | Durachol from Sterling Knight Pharmaceuticals,LLC |
LABELER NAME: | Sterling Knight Pharmaceuticals,LLC |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 3775; 1([iU]/1; mg/1) |
START MARKETING DATE: | 2014-11-16 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 69336-300_27cabc63-3401-4cd8-ae52-e1d8cea28af4 |
PRODUCT NDC: | 69336-300 |
APPLICATION NUMBER: | |
Other CHOLECALCIFEROL; FOLIC ACID Pharmaceutical Manufacturers / Labelers: