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Polibar ACB
Polibar ACB - 32909-804-01 - (BARIUM SULFATE)
Drug Information of Polibar ACB
| Product NDC: | 32909-804 |
| Proprietary Name: | Polibar ACB |
| Non Proprietary Name: | BARIUM SULFATE |
| Active Ingredient(s): | 965 mg/g & nbsp; BARIUM SULFATE |
| Administration Route(s): | RECTAL |
| Dosage Form(s): | POWDER, FOR SUSPENSION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Polibar ACB
| Product NDC: | 32909-804 |
| Labeler Name: | E-Z-EM Canada Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 19780415 |
Package Information of Polibar ACB
| Package NDC: | 32909-804-01 |
| Package Description: | 397 g in 1 BAG (32909-804-01) |
NDC Information of Polibar ACB
| NDC Code | 32909-804-01 |
| Proprietary Name | Polibar ACB |
| Package Description | 397 g in 1 BAG (32909-804-01) |
| Product NDC | 32909-804 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | BARIUM SULFATE |
| Dosage Form Name | POWDER, FOR SUSPENSION |
| Route Name | RECTAL |
| Start Marketing Date | 19780415 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | E-Z-EM Canada Inc |
| Substance Name | BARIUM SULFATE |
| Strength Number | 965 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |
