Nite time - 49348-741-02 - (Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine Succinate)

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Drug Information of Nite time

Product NDC: 49348-741
Proprietary Name: Nite time
Non Proprietary Name: Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine Succinate
Active Ingredient(s): 325; 15; 6.25    mg/1; mg/1; mg/1 & nbsp;   Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine Succinate
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, LIQUID FILLED
Coding System: National Drug Codes(NDC)

Labeler Information of Nite time

Product NDC: 49348-741
Labeler Name: McKesson (Sunmark)
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20120718

Package Information of Nite time

Package NDC: 49348-741-02
Package Description: 1 BLISTER PACK in 1 CARTON (49348-741-02) > 12 CAPSULE, LIQUID FILLED in 1 BLISTER PACK

NDC Information of Nite time

NDC Code 49348-741-02
Proprietary Name Nite time
Package Description 1 BLISTER PACK in 1 CARTON (49348-741-02) > 12 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
Product NDC 49348-741
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine Succinate
Dosage Form Name CAPSULE, LIQUID FILLED
Route Name ORAL
Start Marketing Date 20120718
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name McKesson (Sunmark)
Substance Name ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; DOXYLAMINE SUCCINATE
Strength Number 325; 15; 6.25
Strength Unit mg/1; mg/1; mg/1
Pharmaceutical Classes

Complete Information of Nite time


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