Home > National Drug Code (NDC) > Acetaminophen

Acetaminophen - 0615-4510-39 - (Acetaminophen)

Alphabetical Index


Drug Information of Acetaminophen

Product NDC: 0615-4510
Proprietary Name: Acetaminophen
Non Proprietary Name: Acetaminophen
Active Ingredient(s): 500    mg/1 & nbsp;   Acetaminophen
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Acetaminophen

Product NDC: 0615-4510
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: 20121004

Package Information of Acetaminophen

Package NDC: 0615-4510-39
Package Description: 30 TABLET in 1 BLISTER PACK (0615-4510-39)

NDC Information of Acetaminophen

NDC Code 0615-4510-39
Proprietary Name Acetaminophen
Package Description 30 TABLET in 1 BLISTER PACK (0615-4510-39)
Product NDC 0615-4510
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20121004
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name NCS HealthCare of KY, Inc dba Vangard Labs
Substance Name ACETAMINOPHEN
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Acetaminophen


General Information