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Day Time PE - 49348-738-02 - (ACETAMINOHPEN, DEXTROMETHORPHAN HBr, PHENYLEPHRINE HCl)

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Drug Information of Day Time PE

Product NDC: 49348-738
Proprietary Name: Day Time PE
Non Proprietary Name: ACETAMINOHPEN, DEXTROMETHORPHAN HBr, PHENYLEPHRINE HCl
Active Ingredient(s): 325; 10; 5    mg/1; mg/1; mg/1 & nbsp;   ACETAMINOHPEN, DEXTROMETHORPHAN HBr, PHENYLEPHRINE HCl
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, LIQUID FILLED
Coding System: National Drug Codes(NDC)

Labeler Information of Day Time PE

Product NDC: 49348-738
Labeler Name: McKesson (Sunmark)
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20100709

Package Information of Day Time PE

Package NDC: 49348-738-02
Package Description: 1 BLISTER PACK in 1 CARTON (49348-738-02) > 12 CAPSULE, LIQUID FILLED in 1 BLISTER PACK

NDC Information of Day Time PE

NDC Code 49348-738-02
Proprietary Name Day Time PE
Package Description 1 BLISTER PACK in 1 CARTON (49348-738-02) > 12 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
Product NDC 49348-738
Product Type Name HUMAN OTC DRUG
Non Proprietary Name ACETAMINOHPEN, DEXTROMETHORPHAN HBr, PHENYLEPHRINE HCl
Dosage Form Name CAPSULE, LIQUID FILLED
Route Name ORAL
Start Marketing Date 20100709
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name McKesson (Sunmark)
Substance Name ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE HYDROCHLORIDE
Strength Number 325; 10; 5
Strength Unit mg/1; mg/1; mg/1
Pharmaceutical Classes

Complete Information of Day Time PE


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