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Gastrografin - 0270-0445-35 - (diatrizoate meglumine and diatrizoate sodium)

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Drug Information of Gastrografin

Product NDC: 0270-0445
Proprietary Name: Gastrografin
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): ORAL; RECTAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of Gastrografin

Product NDC: 0270-0445
Labeler Name: BRACCO DIAGNOSTICS INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA011245
Marketing Category: NDA
Start Marketing Date: 19580226

Package Information of Gastrografin

Package NDC: 0270-0445-35
Package Description: 24 BOTTLE in 1 BOX (0270-0445-35) > 30 mL in 1 BOTTLE

NDC Information of Gastrografin

NDC Code 0270-0445-35
Proprietary Name Gastrografin
Package Description 24 BOTTLE in 1 BOX (0270-0445-35) > 30 mL in 1 BOTTLE
Product NDC 0270-0445
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name diatrizoate meglumine and diatrizoate sodium
Dosage Form Name LIQUID
Route Name ORAL; RECTAL
Start Marketing Date 19580226
Marketing Category Name NDA
Labeler Name BRACCO DIAGNOSTICS 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]

Complete Information of Gastrografin


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