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MD-76R
MD-76R - 0019-1317-07 - (Diatrizoate meglumine and Diatrizoate sodium)
Drug Information of MD-76R
| Product NDC: | 0019-1317 |
| Proprietary Name: | MD-76R |
| Non Proprietary Name: | Diatrizoate meglumine and Diatrizoate sodium |
| Active Ingredient(s): | 660; 100 mg/mL; mg/mL & nbsp; Diatrizoate meglumine and Diatrizoate sodium |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of MD-76R
| Product NDC: | 0019-1317 |
| Labeler Name: | Mallinckrodt Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA019292 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19890929 |
Package Information of MD-76R
| Package NDC: | 0019-1317-07 |
| Package Description: | 12 BOTTLE, GLASS in 1 BOX (0019-1317-07) > 100 mL in 1 BOTTLE, GLASS |
NDC Information of MD-76R
| NDC Code | 0019-1317-07 |
| Proprietary Name | MD-76R |
| Package Description | 12 BOTTLE, GLASS in 1 BOX (0019-1317-07) > 100 mL in 1 BOTTLE, GLASS |
| Product NDC | 0019-1317 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Diatrizoate meglumine and Diatrizoate sodium |
| Dosage Form Name | SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 19890929 |
| Marketing Category Name | NDA |
| Labeler Name | Mallinckrodt Inc. |
| Substance Name | DIATRIZOATE MEGLUMINE; DIATRIZOATE SODIUM |
| Strength Number | 660; 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] |
