Product NDC: | 0019-4816 |
Proprietary Name: | MD-GASTROVIEW |
Non Proprietary Name: | diatrizoate meglumine and diatrizoate sodium |
Active Ingredient(s): | 600; 100 mg/mL; mg/mL & nbsp; diatrizoate meglumine and diatrizoate sodium |
Administration Route(s): | ORAL; RECTAL |
Dosage Form(s): | SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0019-4816 |
Labeler Name: | Mallinckrodt Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA087388 |
Marketing Category: | ANDA |
Start Marketing Date: | 20090831 |
Package NDC: | 0019-4816-04 |
Package Description: | 25 BOTTLE, GLASS in 1 BOX (0019-4816-04) > 30 mL in 1 BOTTLE, GLASS |
NDC Code | 0019-4816-04 |
Proprietary Name | MD-GASTROVIEW |
Package Description | 25 BOTTLE, GLASS in 1 BOX (0019-4816-04) > 30 mL in 1 BOTTLE, GLASS |
Product NDC | 0019-4816 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | diatrizoate meglumine and diatrizoate sodium |
Dosage Form Name | SOLUTION |
Route Name | ORAL; RECTAL |
Start Marketing Date | 20090831 |
Marketing Category Name | ANDA |
Labeler Name | Mallinckrodt Inc. |
Substance Name | DIATRIZOATE MEGLUMINE; DIATRIZOATE SODIUM |
Strength Number | 600; 100 |
Strength Unit | mg/mL; mg/mL |
Pharmaceutical Classes | Radiographic Contrast Agent [EPC],X-Ray Contrast Activity [MoA],Radiographic Contrast Agent [EPC],X-Ray Contrast Activity [MoA] |