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 Description | Actonel from Allergan, Inc. |
LABELER NAME: | Allergan, Inc. |
DEA SCHEDULE: |
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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: