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Acetaminophen - 55154-0746-9 - (Acetaminophen)

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Drug Information of Acetaminophen

Product NDC: 55154-0746
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: 55154-0746
Labeler Name: Cardinal Health
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20110531

Package Information of Acetaminophen

Package NDC: 55154-0746-9
Package Description: 6 BLISTER PACK in 1 CARTON (55154-0746-9) > 5 TABLET in 1 BLISTER PACK

NDC Information of Acetaminophen

NDC Code 55154-0746-9
Proprietary Name Acetaminophen
Package Description 6 BLISTER PACK in 1 CARTON (55154-0746-9) > 5 TABLET in 1 BLISTER PACK
Product NDC 55154-0746
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110531
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name Cardinal Health
Substance Name ACETAMINOPHEN
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Acetaminophen


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