NIACIN (Sun Pharma Global FZE)
Welcome to the PulseAid listing for the NIACIN drug offered from Sun Pharma Global FZE. This Nicotinic Acid [EPC],Nicotinic Acids [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: | Sun Pharma Global FZE |
NON-PROPRIETARY NAME: | NIACIN |
SUBSTANCE NAME: | NIACIN |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | Nicotinic Acid [EPC],Nicotinic Acids [Chemical/Ingredient] |
ROUTE: | ORAL |
DOSAGE FORM: | TABLET, FILM COATED, EXTENDED RELEASE |
MARKETING CATEGORY NAME: | ANDA |
START MARKETING DATE: | 2014-06-27 |
END MARKETING DATE: | 0000-00-00 |
NIACIN HUMAN PRESCRIPTION DRUG Details:
Item Description | NIACIN from Sun Pharma Global FZE |
LABELER NAME: | Sun Pharma Global FZE |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 500(mg/1) |
START MARKETING DATE: | 2014-06-27 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 47335-539_f9dce906-03c1-4834-93ff-cb0697256c54 |
PRODUCT NDC: | 47335-539 |
APPLICATION NUMBER: | ANDA200484 |
Other NIACIN Pharmaceutical Manufacturers / Labelers: