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Guaiasorb DM - 57896-756-04 - (Dextromethorphan Hydrobromide and Guaifenesin)

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Drug Information of Guaiasorb DM

Product NDC: 57896-756
Proprietary Name: Guaiasorb 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 Guaiasorb DM

Product NDC: 57896-756
Labeler Name: Geri-Care Pharmaceuticals, Corp
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 19950905

Package Information of Guaiasorb DM

Package NDC: 57896-756-04
Package Description: 118 mL in 1 BOTTLE, PLASTIC (57896-756-04)

NDC Information of Guaiasorb DM

NDC Code 57896-756-04
Proprietary Name Guaiasorb DM
Package Description 118 mL in 1 BOTTLE, PLASTIC (57896-756-04)
Product NDC 57896-756
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Dextromethorphan Hydrobromide and Guaifenesin
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 19950905
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Geri-Care Pharmaceuticals, Corp
Substance Name DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN
Strength Number 10; 100
Strength Unit mg/5mL; mg/5mL
Pharmaceutical Classes

Complete Information of Guaiasorb DM


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