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Leader Day Time - 37205-705-62 - (Acetaminophen, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride)

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Drug Information of Leader Day Time

Product NDC: 37205-705
Proprietary Name: Leader Day Time
Non Proprietary Name: Acetaminophen, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride
Active Ingredient(s): 325; 10; 5    mg/1; mg/1; mg/1 & nbsp;   Acetaminophen, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, LIQUID FILLED
Coding System: National Drug Codes(NDC)

Labeler Information of Leader Day Time

Product NDC: 37205-705
Labeler Name: Cardinal Health
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20061006

Package Information of Leader Day Time

Package NDC: 37205-705-62
Package Description: 2 BLISTER PACK in 1 CARTON (37205-705-62) > 12 CAPSULE, LIQUID FILLED in 1 BLISTER PACK

NDC Information of Leader Day Time

NDC Code 37205-705-62
Proprietary Name Leader Day Time
Package Description 2 BLISTER PACK in 1 CARTON (37205-705-62) > 12 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
Product NDC 37205-705
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride
Dosage Form Name CAPSULE, LIQUID FILLED
Route Name ORAL
Start Marketing Date 20061006
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Cardinal Health
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 Leader Day Time


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