| 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 |