Boniva - 0004-0186-82 - (ibandronate sodium)

Alphabetical Index


Drug Information of Boniva

Product NDC: 0004-0186
Proprietary Name: Boniva
Non Proprietary Name: ibandronate sodium
Active Ingredient(s): 150    mg/1 & nbsp;   ibandronate sodium
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Boniva

Product NDC: 0004-0186
Labeler Name: Genentech, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021455
Marketing Category: NDA
Start Marketing Date: 20020715

Package Information of Boniva

Package NDC: 0004-0186-82
Package Description: 3 BLISTER PACK in 1 BOX (0004-0186-82) > 1 TABLET, FILM COATED in 1 BLISTER PACK

NDC Information of Boniva

NDC Code 0004-0186-82
Proprietary Name Boniva
Package Description 3 BLISTER PACK in 1 BOX (0004-0186-82) > 1 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC 0004-0186
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ibandronate sodium
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20020715
Marketing Category Name NDA
Labeler Name Genentech, Inc.
Substance Name IBANDRONATE SODIUM
Strength Number 150
Strength Unit mg/1
Pharmaceutical Classes Bisphosphonate [EPC],Diphosphonates [Chemical/Ingredient]

Complete Information of Boniva


General Information