Home > National Drug Code (NDC) > Regular Strength Pain Relief

Regular Strength Pain Relief - 57896-101-10 - (Acetaminophen)

Alphabetical Index


Drug Information of Regular Strength Pain Relief

Product NDC: 57896-101
Proprietary Name: Regular Strength Pain Relief
Non Proprietary Name: Acetaminophen
Active Ingredient(s): 325    mg/1 & nbsp;   Acetaminophen
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Regular Strength Pain Relief

Product NDC: 57896-101
Labeler Name: Geri-Care Pharmaceutical Corp
Product Type: HUMAN OTC DRUG
FDA Application Number: part343
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 19890101

Package Information of Regular Strength Pain Relief

Package NDC: 57896-101-10
Package Description: 1000 TABLET in 1 BOTTLE (57896-101-10)

NDC Information of Regular Strength Pain Relief

NDC Code 57896-101-10
Proprietary Name Regular Strength Pain Relief
Package Description 1000 TABLET in 1 BOTTLE (57896-101-10)
Product NDC 57896-101
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19890101
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Geri-Care Pharmaceutical Corp
Substance Name ACETAMINOPHEN
Strength Number 325
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Regular Strength Pain Relief


General Information