ACTONEL - 0149-0472-02 - (RISEDRONATE SODIUM)

Alphabetical Index


Drug Information of ACTONEL

Product NDC: 0149-0472
Proprietary Name: ACTONEL
Non Proprietary Name: RISEDRONATE SODIUM
Active Ingredient(s): 35    mg/1 & nbsp;   RISEDRONATE SODIUM
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of ACTONEL

Product NDC: 0149-0472
Labeler Name: Warner Chilcott Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020835
Marketing Category: NDA
Start Marketing Date: 20020517

Package Information of ACTONEL

Package NDC: 0149-0472-02
Package Description: 36 DOSE PACK in 1 CASE (0149-0472-02) > 1 TRAY in 1 DOSE PACK > 1 TABLET, FILM COATED in 1 TRAY

NDC Information of ACTONEL

NDC Code 0149-0472-02
Proprietary Name ACTONEL
Package Description 36 DOSE PACK in 1 CASE (0149-0472-02) > 1 TRAY in 1 DOSE PACK > 1 TABLET, FILM COATED in 1 TRAY
Product NDC 0149-0472
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name RISEDRONATE SODIUM
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20020517
Marketing Category Name NDA
Labeler Name Warner Chilcott Pharmaceuticals Inc.
Substance Name RISEDRONATE SODIUM
Strength Number 35
Strength Unit mg/1
Pharmaceutical Classes Bisphosphonate [EPC],Diphosphonates [Chemical/Ingredient]

Complete Information of ACTONEL


General Information