ConRx Cold - 68737-232-16 - (Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, and Phenylephrine Hydrochloride)

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Drug Information of ConRx Cold

Product NDC: 68737-232
Proprietary Name: ConRx Cold
Non Proprietary Name: Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, and Phenylephrine Hydrochloride
Active Ingredient(s): 325; 10; 200; 5    mg/1; mg/1; mg/1; mg/1 & nbsp;   Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, and Phenylephrine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of ConRx Cold

Product NDC: 68737-232
Labeler Name: Eagle Distributors,Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20130215

Package Information of ConRx Cold

Package NDC: 68737-232-16
Package Description: 50 POUCH in 1 BOX (68737-232-16) > 2 TABLET in 1 POUCH

NDC Information of ConRx Cold

NDC Code 68737-232-16
Proprietary Name ConRx Cold
Package Description 50 POUCH in 1 BOX (68737-232-16) > 2 TABLET in 1 POUCH
Product NDC 68737-232
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, and Phenylephrine Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130215
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Eagle Distributors,Inc.
Substance Name ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE
Strength Number 325; 10; 200; 5
Strength Unit mg/1; mg/1; mg/1; mg/1
Pharmaceutical Classes

Complete Information of ConRx Cold


General Information