| Product NDC: | 32909-652 |
| Proprietary Name: | E-Z-Dose with Liquid Polibar Plus |
| Non Proprietary Name: | Barium Sulfate Suspension |
| Active Ingredient(s): | 1.05 g/mL & nbsp; Barium Sulfate Suspension |
| Administration Route(s): | RECTAL |
| Dosage Form(s): | SUSPENSION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 32909-652 |
| Labeler Name: | E-Z-EM Canada Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 19840801 |
| Package NDC: | 32909-652-02 |
| Package Description: | 1 BOTTLE, DISPENSING in 1 KIT (32909-652-02) > 650 mL in 1 BOTTLE, DISPENSING |
| NDC Code | 32909-652-02 |
| Proprietary Name | E-Z-Dose with Liquid Polibar Plus |
| Package Description | 1 BOTTLE, DISPENSING in 1 KIT (32909-652-02) > 650 mL in 1 BOTTLE, DISPENSING |
| Product NDC | 32909-652 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Barium Sulfate Suspension |
| Dosage Form Name | SUSPENSION |
| Route Name | RECTAL |
| Start Marketing Date | 19840801 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | E-Z-EM Canada Inc |
| Substance Name | BARIUM SULFATE |
| Strength Number | 1.05 |
| Strength Unit | g/mL |
| Pharmaceutical Classes |