| 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: | 32909-186-01 |
| Package Description: | 1900 mL in 1 JUG (32909-186-01) |
| NDC Code | 32909-186-01 |
| Proprietary Name | LIQUID E-Z-PAQUE |
| Package Description | 1900 mL in 1 JUG (32909-186-01) |
| 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 |