Product NDC: | 32909-186 |
Proprietary Name: | LIQUID E-Z-PAQUE |
Non Proprietary Name: | barium sulfate |
Active Ingredient(s): | .6 g/mL & nbsp; barium sulfate |
Administration Route(s): | ORAL |
Dosage Form(s): | SUSPENSION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 32909-186 |
Labeler Name: | E-Z-EM Canada Inc |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 19841101 |
Package NDC: | 32909-186-02 |
Package Description: | 355 mL in 1 BOTTLE (32909-186-02) |
NDC Code | 32909-186-02 |
Proprietary Name | LIQUID E-Z-PAQUE |
Package Description | 355 mL in 1 BOTTLE (32909-186-02) |
Product NDC | 32909-186 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | barium sulfate |
Dosage Form Name | SUSPENSION |
Route Name | ORAL |
Start Marketing Date | 19841101 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Labeler Name | E-Z-EM Canada Inc |
Substance Name | BARIUM SULFATE |
Strength Number | .6 |
Strength Unit | g/mL |
Pharmaceutical Classes |