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E-Z-HD
E-Z-HD - 32909-764-01 - (Barium Sulfate)
Drug Information of E-Z-HD
| Product NDC: | 32909-764 |
| Proprietary Name: | E-Z-HD |
| Non Proprietary Name: | Barium Sulfate |
| Active Ingredient(s): | 980 mg/g & nbsp; Barium Sulfate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | POWDER, FOR SUSPENSION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of E-Z-HD
| Product NDC: | 32909-764 |
| Labeler Name: | E-Z-EM Canada Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 19800615 |
Package Information of E-Z-HD
| Package NDC: | 32909-764-01 |
| Package Description: | 340 g in 1 BOTTLE (32909-764-01) |
NDC Information of E-Z-HD
| NDC Code | 32909-764-01 |
| Proprietary Name | E-Z-HD |
| Package Description | 340 g in 1 BOTTLE (32909-764-01) |
| Product NDC | 32909-764 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Barium Sulfate |
| Dosage Form Name | POWDER, FOR SUSPENSION |
| Route Name | ORAL |
| Start Marketing Date | 19800615 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | E-Z-EM Canada Inc |
| Substance Name | BARIUM SULFATE |
| Strength Number | 980 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |
