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MD-GASTROVIEW - 0019-4816-04 - (diatrizoate meglumine and diatrizoate sodium)

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Drug Information of MD-GASTROVIEW

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)

Labeler Information of MD-GASTROVIEW

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 Information of MD-GASTROVIEW

Package NDC: 0019-4816-04
Package Description: 25 BOTTLE, GLASS in 1 BOX (0019-4816-04) > 30 mL in 1 BOTTLE, GLASS

NDC Information of MD-GASTROVIEW

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]

Complete Information of MD-GASTROVIEW


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