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Guaiatussin AC - 50383-087-16 - (guaifenesin and codeine phosphate)

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Drug Information of Guaiatussin AC

Product NDC: 50383-087
Proprietary Name: Guaiatussin AC
Non Proprietary Name: guaifenesin and codeine phosphate
Active Ingredient(s): 10; 100    mg/5mL; mg/5mL & nbsp;   guaifenesin and codeine phosphate
Administration Route(s): ORAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of Guaiatussin AC

Product NDC: 50383-087
Labeler Name: Hi-Tech Pharmacal Co., Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20100908

Package Information of Guaiatussin AC

Package NDC: 50383-087-16
Package Description: 473 mL in 1 BOTTLE (50383-087-16)

NDC Information of Guaiatussin AC

NDC Code 50383-087-16
Proprietary Name Guaiatussin AC
Package Description 473 mL in 1 BOTTLE (50383-087-16)
Product NDC 50383-087
Product Type Name HUMAN OTC DRUG
Non Proprietary Name guaifenesin and codeine phosphate
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 20100908
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Hi-Tech Pharmacal Co., Inc.
Substance Name CODEINE PHOSPHATE; GUAIFENESIN
Strength Number 10; 100
Strength Unit mg/5mL; mg/5mL
Pharmaceutical Classes

Complete Information of Guaiatussin AC


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