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 |