Home > National Drug Code (NDC) > Preferred Plus Extra Strength Pain Relief

Preferred Plus Extra Strength Pain Relief - 61715-052-01 - (Acetaminophen)

Alphabetical Index


Drug Information of Preferred Plus Extra Strength Pain Relief

Product NDC: 61715-052
Proprietary Name: Preferred Plus Extra Strength Pain Relief
Non Proprietary Name: Acetaminophen
Active Ingredient(s): 500    mg/1 & nbsp;   Acetaminophen
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Preferred Plus Extra Strength Pain Relief

Product NDC: 61715-052
Labeler Name: Kinray
Product Type: HUMAN OTC DRUG
FDA Application Number: part343
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20130626

Package Information of Preferred Plus Extra Strength Pain Relief

Package NDC: 61715-052-01
Package Description: 1 TABLET in 1 CARTON (61715-052-01)

NDC Information of Preferred Plus Extra Strength Pain Relief

NDC Code 61715-052-01
Proprietary Name Preferred Plus Extra Strength Pain Relief
Package Description 1 TABLET in 1 CARTON (61715-052-01)
Product NDC 61715-052
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130626
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Kinray
Substance Name ACETAMINOPHEN
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Preferred Plus Extra Strength Pain Relief


General Information