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Acetaminophen - 0363-0340-80 - (Acetaminophen)

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Drug Information of Acetaminophen

Product NDC: 0363-0340
Proprietary Name: Acetaminophen
Non Proprietary Name: Acetaminophen
Active Ingredient(s): 650    mg/1 & nbsp;   Acetaminophen
Administration Route(s): ORAL
Dosage Form(s): TABLET, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Acetaminophen

Product NDC: 0363-0340
Labeler Name: Walgreen Company
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA078569
Marketing Category: ANDA
Start Marketing Date: 20121221

Package Information of Acetaminophen

Package NDC: 0363-0340-80
Package Description: 80 TABLET, EXTENDED RELEASE in 1 BOTTLE (0363-0340-80)

NDC Information of Acetaminophen

NDC Code 0363-0340-80
Proprietary Name Acetaminophen
Package Description 80 TABLET, EXTENDED RELEASE in 1 BOTTLE (0363-0340-80)
Product NDC 0363-0340
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20121221
Marketing Category Name ANDA
Labeler Name Walgreen Company
Substance Name ACETAMINOPHEN
Strength Number 650
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Acetaminophen


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