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acetaminophen - 45802-730-32 - (Acetaminophen)

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Drug Information of acetaminophen

Product NDC: 45802-730
Proprietary Name: acetaminophen
Non Proprietary Name: Acetaminophen
Active Ingredient(s): 650    mg/1 & nbsp;   Acetaminophen
Administration Route(s): RECTAL
Dosage Form(s): SUPPOSITORY
Coding System: National Drug Codes(NDC)

Labeler Information of acetaminophen

Product NDC: 45802-730
Labeler Name: Perrigo New York Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA070608
Marketing Category: ANDA
Start Marketing Date: 20101028

Package Information of acetaminophen

Package NDC: 45802-730-32
Package Description: 10 BLISTER PACK in 1 CARTON (45802-730-32) > 5 SUPPOSITORY in 1 BLISTER PACK

NDC Information of acetaminophen

NDC Code 45802-730-32
Proprietary Name acetaminophen
Package Description 10 BLISTER PACK in 1 CARTON (45802-730-32) > 5 SUPPOSITORY in 1 BLISTER PACK
Product NDC 45802-730
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen
Dosage Form Name SUPPOSITORY
Route Name RECTAL
Start Marketing Date 20101028
Marketing Category Name ANDA
Labeler Name Perrigo New York Inc
Substance Name ACETAMINOPHEN
Strength Number 650
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of acetaminophen


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