Product NDC: | 65649-102 |
Proprietary Name: | GIAZO |
Non Proprietary Name: | balsalazide disodium |
Active Ingredient(s): | 1.1 g/1 & nbsp; balsalazide disodium |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, FILM COATED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 65649-102 |
Labeler Name: | Salix Pharmaceuticals, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA022205 |
Marketing Category: | NDA |
Start Marketing Date: | 20120202 |
Package NDC: | 65649-102-02 |
Package Description: | 180 TABLET, FILM COATED in 1 BOTTLE (65649-102-02) |
NDC Code | 65649-102-02 |
Proprietary Name | GIAZO |
Package Description | 180 TABLET, FILM COATED in 1 BOTTLE (65649-102-02) |
Product NDC | 65649-102 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | balsalazide disodium |
Dosage Form Name | TABLET, FILM COATED |
Route Name | ORAL |
Start Marketing Date | 20120202 |
Marketing Category Name | NDA |
Labeler Name | Salix Pharmaceuticals, Inc. |
Substance Name | BALSALAZIDE DISODIUM |
Strength Number | 1.1 |
Strength Unit | g/1 |
Pharmaceutical Classes | Aminosalicylate [EPC],Aminosalicylic Acids [Chemical/Ingredient] |