Actonel (Allergan, Inc.)


Welcome to the PulseAid listing for the Actonel drug offered from Allergan, Inc.. This Bisphosphonate [EPC],Diphosphonates [Chemical/Ingredient],Bisphosphonate [EPC],Diphosphonates [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: Allergan, Inc.
NON-PROPRIETARY NAME: Risedronate Sodium
SUBSTANCE NAME: RISEDRONATE SODIUM HEMI-PENTAHYDRATE; RISEDRONATE SODIUM MONOHYDRATE
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: Bisphosphonate [EPC],Diphosphonates [Chemical/Ingredient],Bisphosphonate [EPC],Diphosphonates [Chemical/Ingredient]
ROUTE: ORAL
DOSAGE FORM: TABLET, FILM COATED
MARKETING CATEGORY NAME: NDA
START MARKETING DATE: 1998-03-27
END MARKETING DATE: 0000-00-00


Actonel HUMAN PRESCRIPTION DRUG Details:

Item DescriptionActonel from Allergan, Inc.
LABELER NAME: Allergan, Inc.
DEA SCHEDULE:
ACTIVE STRENGTH: 25.8; 4.2(mg/1; mg/1)
START MARKETING DATE: 1998-03-27
END MARKETING DATE: 0000-00-00
PRODUCT ID: 0430-0470_6601a365-a4ea-430b-903b-b3139a944fa2
PRODUCT NDC: 0430-0470
APPLICATION NUMBER: NDA020835

Other RISEDRONATE SODIUM HEMI-PENTAHYDRATE; RISEDRONATE SODIUM MONOHYDRATE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Actavis Pharma, Inc.Risedronate Sodium
Allergan, Inc.Actonel
Warner Chilcott (US), LLCAtelvia