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ACETAMINOPHEN - 49483-342-01 - (ACETAMINOPHEN)

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Drug Information of ACETAMINOPHEN

Product NDC: 49483-342
Proprietary Name: ACETAMINOPHEN
Non Proprietary Name: ACETAMINOPHEN
Active Ingredient(s): 500    mg/1 & nbsp;   ACETAMINOPHEN
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of ACETAMINOPHEN

Product NDC: 49483-342
Labeler Name: TIME CAP LABORATORIES, INC
Product Type: HUMAN OTC DRUG
FDA Application Number: part343
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20120501

Package Information of ACETAMINOPHEN

Package NDC: 49483-342-01
Package Description: 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (49483-342-01)

NDC Information of ACETAMINOPHEN

NDC Code 49483-342-01
Proprietary Name ACETAMINOPHEN
Package Description 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (49483-342-01)
Product NDC 49483-342
Product Type Name HUMAN OTC DRUG
Non Proprietary Name ACETAMINOPHEN
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20120501
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name TIME CAP LABORATORIES, INC
Substance Name ACETAMINOPHEN
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of ACETAMINOPHEN


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