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acetaminophen - 55312-544-71 - (Acetaminophen)

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Drug Information of acetaminophen

Product NDC: 55312-544
Proprietary Name: acetaminophen
Non Proprietary Name: Acetaminophen
Active Ingredient(s): 650    mg/1 & nbsp;   Acetaminophen
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of acetaminophen

Product NDC: 55312-544
Labeler Name: Western Family Foods Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA075077
Marketing Category: ANDA
Start Marketing Date: 20060320

Package Information of acetaminophen

Package NDC: 55312-544-71
Package Description: 1 BOTTLE in 1 CARTON (55312-544-71) > 50 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE

NDC Information of acetaminophen

NDC Code 55312-544-71
Proprietary Name acetaminophen
Package Description 1 BOTTLE in 1 CARTON (55312-544-71) > 50 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE
Product NDC 55312-544
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen
Dosage Form Name TABLET, FILM COATED, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20060320
Marketing Category Name ANDA
Labeler Name Western Family Foods Inc
Substance Name ACETAMINOPHEN
Strength Number 650
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of acetaminophen


General Information