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Junior Strength Pain Relief - 66007-145-02 - (Acetaminophen)

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Drug Information of Junior Strength Pain Relief

Product NDC: 66007-145
Proprietary Name: Junior Strength Pain Relief
Non Proprietary Name: Acetaminophen
Active Ingredient(s): 160    mg/1 & nbsp;   Acetaminophen
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Junior Strength Pain Relief

Product NDC: 66007-145
Labeler Name: Capricorn Pharma Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part343
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20100726

Package Information of Junior Strength Pain Relief

Package NDC: 66007-145-02
Package Description: 4 BLISTER PACK in 1 CARTON (66007-145-02) > 6 TABLET in 1 BLISTER PACK (66007-145-01)

NDC Information of Junior Strength Pain Relief

NDC Code 66007-145-02
Proprietary Name Junior Strength Pain Relief
Package Description 4 BLISTER PACK in 1 CARTON (66007-145-02) > 6 TABLET in 1 BLISTER PACK (66007-145-01)
Product NDC 66007-145
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100726
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Capricorn Pharma Inc.
Substance Name ACETAMINOPHEN
Strength Number 160
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Junior Strength Pain Relief


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