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Acetaminophen - 0615-4554-67 - (Acetaminophen)

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Drug Information of Acetaminophen

Product NDC: 0615-4554
Proprietary Name: Acetaminophen
Non Proprietary Name: Acetaminophen
Active Ingredient(s): 325    mg/1 & nbsp;   Acetaminophen
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Acetaminophen

Product NDC: 0615-4554
Labeler Name: NCS HealthCare of KY, Inc dba Vangard Labs
Product Type: HUMAN OTC DRUG
FDA Application Number: part343
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20100804

Package Information of Acetaminophen

Package NDC: 0615-4554-67
Package Description: 60 TABLET in 1 BLISTER PACK (0615-4554-67)

NDC Information of Acetaminophen

NDC Code 0615-4554-67
Proprietary Name Acetaminophen
Package Description 60 TABLET in 1 BLISTER PACK (0615-4554-67)
Product NDC 0615-4554
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100804
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name NCS HealthCare of KY, Inc dba Vangard Labs
Substance Name ACETAMINOPHEN
Strength Number 325
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Acetaminophen


General Information