Product NDC: | 32909-727 |
Proprietary Name: | E-Z-CAT DRY |
Non Proprietary Name: | Barium Sulfate |
Active Ingredient(s): | 9.5 g/23g & nbsp; Barium Sulfate |
Administration Route(s): | ORAL |
Dosage Form(s): | POWDER, FOR SUSPENSION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 32909-727 |
Labeler Name: | E-Z-EM Canada Inc |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 19960101 |
Package NDC: | 32909-727-01 |
Package Description: | 50 POUCH in 1 BOX (32909-727-01) > 23 g in 1 POUCH |
NDC Code | 32909-727-01 |
Proprietary Name | E-Z-CAT DRY |
Package Description | 50 POUCH in 1 BOX (32909-727-01) > 23 g in 1 POUCH |
Product NDC | 32909-727 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Barium Sulfate |
Dosage Form Name | POWDER, FOR SUSPENSION |
Route Name | ORAL |
Start Marketing Date | 19960101 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Labeler Name | E-Z-EM Canada Inc |
Substance Name | BARIUM SULFATE |
Strength Number | 9.5 |
Strength Unit | g/23g |
Pharmaceutical Classes |