ALAVERT ALLERGY SINUS D-12 (Wyeth Consumer Healthcare)
Welcome to the PulseAid listing for the ALAVERT ALLERGY SINUS D-12 drug offered from Wyeth Consumer Healthcare. This pharmaceutical is classified as a HUMAN OTC 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 OTC DRUG drug type category.
LABELER NAME / MANUFACTURER: | Wyeth Consumer Healthcare |
NON-PROPRIETARY NAME: | loratadine, pseudoephedrine sulfate |
SUBSTANCE NAME: | LORATADINE; PSEUDOEPHEDRINE SULFATE |
TYPE: | HUMAN OTC DRUG |
PHARMA CLASS: | |
ROUTE: | ORAL |
DOSAGE FORM: | TABLET, FILM COATED, EXTENDED RELEASE |
MARKETING CATEGORY NAME: | ANDA |
START MARKETING DATE: | 2004-01-30 |
END MARKETING DATE: | 0000-00-00 |
ALAVERT ALLERGY SINUS D-12 HUMAN OTC DRUG Details:
Item Description | ALAVERT ALLERGY SINUS D-12 from Wyeth Consumer Healthcare |
LABELER NAME: | Wyeth Consumer Healthcare |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 5; 120(mg/1; mg/1) |
START MARKETING DATE: | 2004-01-30 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 0573-2660_91ed3e9a-e637-bfd9-e403-eef89c2c6816 |
PRODUCT NDC: | 0573-2660 |
APPLICATION NUMBER: | ANDA076050 |
Other LORATADINE; PSEUDOEPHEDRINE SULFATE Pharmaceutical Manufacturers / Labelers: