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LEADER iNTENSE COUGH RELIEVER - 37205-610-01 - (Dextromethorphan Hydrobromide / Guaifenesin)

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Drug Information of LEADER iNTENSE COUGH RELIEVER

Product NDC: 37205-610
Proprietary Name: LEADER iNTENSE COUGH RELIEVER
Non Proprietary Name: Dextromethorphan Hydrobromide / Guaifenesin
Active Ingredient(s): 20; 300    mg/5mL; mg/5mL & nbsp;   Dextromethorphan Hydrobromide / Guaifenesin
Administration Route(s): ORAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of LEADER iNTENSE COUGH RELIEVER

Product NDC: 37205-610
Labeler Name: Cardinal Health
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20110802

Package Information of LEADER iNTENSE COUGH RELIEVER

Package NDC: 37205-610-01
Package Description: 1 BOTTLE, PLASTIC in 1 CARTON (37205-610-01) > 120 mL in 1 BOTTLE, PLASTIC (37205-610-26)

NDC Information of LEADER iNTENSE COUGH RELIEVER

NDC Code 37205-610-01
Proprietary Name LEADER iNTENSE COUGH RELIEVER
Package Description 1 BOTTLE, PLASTIC in 1 CARTON (37205-610-01) > 120 mL in 1 BOTTLE, PLASTIC (37205-610-26)
Product NDC 37205-610
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Dextromethorphan Hydrobromide / Guaifenesin
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 20110802
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Cardinal Health
Substance Name DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN
Strength Number 20; 300
Strength Unit mg/5mL; mg/5mL
Pharmaceutical Classes

Complete Information of LEADER iNTENSE COUGH RELIEVER


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