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Ritussin DM - 53807-409-08 - (DEXTROMETHORPHAN HYDROBROMIDE and GUAIFENESIN)

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Drug Information of Ritussin DM

Product NDC: 53807-409
Proprietary Name: Ritussin DM
Non Proprietary Name: DEXTROMETHORPHAN HYDROBROMIDE and GUAIFENESIN
Active Ingredient(s): 10; 100    mg/5mL; mg/5mL & nbsp;   DEXTROMETHORPHAN HYDROBROMIDE and GUAIFENESIN
Administration Route(s): ORAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of Ritussin DM

Product NDC: 53807-409
Labeler Name: Rij Pharmaceutical Corporation
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 19990316

Package Information of Ritussin DM

Package NDC: 53807-409-08
Package Description: 236 mL in 1 BOTTLE (53807-409-08)

NDC Information of Ritussin DM

NDC Code 53807-409-08
Proprietary Name Ritussin DM
Package Description 236 mL in 1 BOTTLE (53807-409-08)
Product NDC 53807-409
Product Type Name HUMAN OTC DRUG
Non Proprietary Name DEXTROMETHORPHAN HYDROBROMIDE and GUAIFENESIN
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 19990316
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Rij Pharmaceutical Corporation
Substance Name DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN
Strength Number 10; 100
Strength Unit mg/5mL; mg/5mL
Pharmaceutical Classes

Complete Information of Ritussin DM


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