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IBANDRONATE SODIUM - 60505-2795-0 - (IBANDRONATE SODIUM)

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Drug Information of IBANDRONATE SODIUM

Product NDC: 60505-2795
Proprietary Name: IBANDRONATE SODIUM
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 IBANDRONATE SODIUM

Product NDC: 60505-2795
Labeler Name: Apotex Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078948
Marketing Category: ANDA
Start Marketing Date: 20120319

Package Information of IBANDRONATE SODIUM

Package NDC: 60505-2795-0
Package Description: 3 BLISTER PACK in 1 PACKAGE (60505-2795-0) > 1 TABLET, FILM COATED in 1 BLISTER PACK

NDC Information of IBANDRONATE SODIUM

NDC Code 60505-2795-0
Proprietary Name IBANDRONATE SODIUM
Package Description 3 BLISTER PACK in 1 PACKAGE (60505-2795-0) > 1 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC 60505-2795
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name IBANDRONATE SODIUM
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20120319
Marketing Category Name ANDA
Labeler Name Apotex Corp
Substance Name IBANDRONATE SODIUM
Strength Number 150
Strength Unit mg/1
Pharmaceutical Classes Bisphosphonate [EPC],Diphosphonates [Chemical/Ingredient]

Complete Information of IBANDRONATE SODIUM


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