Allegra D-12 Hour (sanofi-aventis U.S. LLC)
Welcome to the PulseAid listing for the Allegra D-12 Hour drug offered from sanofi-aventis U.S. LLC. This Histamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Antagonist [EPC],Adrenergic alpha-Agonists [MoA],alpha-Adrenergic Agonist [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: | sanofi-aventis U.S. LLC |
NON-PROPRIETARY NAME: | fexofenadine hydrochloride and pseudoephedrine hydrochloride |
SUBSTANCE NAME: | FEXOFENADINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | Histamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Antagonist [EPC],Adrenergic alpha-Agonists [MoA],alpha-Adrenergic Agonist [EPC] |
ROUTE: | ORAL |
DOSAGE FORM: | TABLET, EXTENDED RELEASE |
MARKETING CATEGORY NAME: | NDA |
START MARKETING DATE: | 1997-12-24 |
END MARKETING DATE: | 0000-00-00 |
Allegra D-12 Hour HUMAN PRESCRIPTION DRUG Details:
Item Description | Allegra D-12 Hour from sanofi-aventis U.S. LLC |
LABELER NAME: | sanofi-aventis U.S. LLC |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 60; 120(mg/1; mg/1) |
START MARKETING DATE: | 1997-12-24 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 0088-1090_0af9d08a-03a2-4626-8049-6822d108c4c0 |
PRODUCT NDC: | 0088-1090 |
APPLICATION NUMBER: | NDA020786 |
Other FEXOFENADINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers: