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Cheratussin AC - 0603-1075-58 - (codeine phosphate and guaifenesin)

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Drug Information of Cheratussin AC

Product NDC: 0603-1075
Proprietary Name: Cheratussin AC
Non Proprietary Name: codeine phosphate and guaifenesin
Active Ingredient(s): 10; 100    mg/5mL; mg/5mL & nbsp;   codeine phosphate and guaifenesin
Administration Route(s): ORAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of Cheratussin AC

Product NDC: 0603-1075
Labeler Name: Qualitest Pharmaceuticals
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 19960901

Package Information of Cheratussin AC

Package NDC: 0603-1075-58
Package Description: 473 mL in 1 BOTTLE, PLASTIC (0603-1075-58)

NDC Information of Cheratussin AC

NDC Code 0603-1075-58
Proprietary Name Cheratussin AC
Package Description 473 mL in 1 BOTTLE, PLASTIC (0603-1075-58)
Product NDC 0603-1075
Product Type Name HUMAN OTC DRUG
Non Proprietary Name codeine phosphate and guaifenesin
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 19960901
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Qualitest Pharmaceuticals
Substance Name CODEINE PHOSPHATE; GUAIFENESIN
Strength Number 10; 100
Strength Unit mg/5mL; mg/5mL
Pharmaceutical Classes

Complete Information of Cheratussin AC


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