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equaline anti nausea - 41163-630-26 - (Dextrose (glucose), Levulose (fructose), Phosphoric Acid)

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Drug Information of equaline anti nausea

Product NDC: 41163-630
Proprietary Name: equaline anti nausea
Non Proprietary Name: Dextrose (glucose), Levulose (fructose), Phosphoric Acid
Active Ingredient(s): 1.87; 1.87; 21.5    g/5mL; g/5mL; mg/5mL & nbsp;   Dextrose (glucose), Levulose (fructose), Phosphoric Acid
Administration Route(s): ORAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of equaline anti nausea

Product NDC: 41163-630
Labeler Name: Supervalu Inc
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20040928

Package Information of equaline anti nausea

Package NDC: 41163-630-26
Package Description: 1 BOTTLE in 1 CARTON (41163-630-26) > 118 mL in 1 BOTTLE

NDC Information of equaline anti nausea

NDC Code 41163-630-26
Proprietary Name equaline anti nausea
Package Description 1 BOTTLE in 1 CARTON (41163-630-26) > 118 mL in 1 BOTTLE
Product NDC 41163-630
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Dextrose (glucose), Levulose (fructose), Phosphoric Acid
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 20040928
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name Supervalu Inc
Substance Name DEXTROSE; FRUCTOSE; PHOSPHORIC ACID
Strength Number 1.87; 1.87; 21.5
Strength Unit g/5mL; g/5mL; mg/5mL
Pharmaceutical Classes

Complete Information of equaline anti nausea


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