Valsartan and Hydrochlorothiazide (Sandoz Inc)
Welcome to the PulseAid listing for the Valsartan and Hydrochlorothiazide drug offered from Sandoz Inc. This Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [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: | Sandoz Inc |
NON-PROPRIETARY NAME: | valsartan and hydrochlorothiazide |
SUBSTANCE NAME: | VALSARTAN; HYDROCHLOROTHIAZIDE |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient] |
ROUTE: | ORAL |
DOSAGE FORM: | TABLET, FILM COATED |
MARKETING CATEGORY NAME: | NDA AUTHORIZED GENERIC |
START MARKETING DATE: | 2012-09-21 |
END MARKETING DATE: | 0000-00-00 |
Valsartan and Hydrochlorothiazide HUMAN PRESCRIPTION DRUG Details:
Item Description | Valsartan and Hydrochlorothiazide from Sandoz Inc |
LABELER NAME: | Sandoz Inc |
DEA SCHEDULE: |
|
ACTIVE STRENGTH: | 80; 12.5(mg/1; mg/1) |
START MARKETING DATE: | 2012-09-21 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 0781-5948_ff7a21b8-e6b1-4111-a48f-143877db39eb |
PRODUCT NDC: | 0781-5948 |
APPLICATION NUMBER: | NDA020818 |
Other VALSARTAN; HYDROCHLOROTHIAZIDE Pharmaceutical Manufacturers / Labelers: