Home > National Drug Code (NDC) > Rapid Release Pain Reliever

Rapid Release Pain Reliever - 21130-519-29 - (Acetaminophen)

Alphabetical Index


Drug Information of Rapid Release Pain Reliever

Product NDC: 21130-519
Proprietary Name: Rapid Release Pain Reliever
Non Proprietary Name: Acetaminophen
Active Ingredient(s): 500    mg/1 & nbsp;   Acetaminophen
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, LIQUID FILLED
Coding System: National Drug Codes(NDC)

Labeler Information of Rapid Release Pain Reliever

Product NDC: 21130-519
Labeler Name: Safeway
Product Type: HUMAN OTC DRUG
FDA Application Number: part343
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20040510

Package Information of Rapid Release Pain Reliever

Package NDC: 21130-519-29
Package Description: 1 BOTTLE, PLASTIC in 1 CARTON (21130-519-29) > 150 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC

NDC Information of Rapid Release Pain Reliever

NDC Code 21130-519-29
Proprietary Name Rapid Release Pain Reliever
Package Description 1 BOTTLE, PLASTIC in 1 CARTON (21130-519-29) > 150 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC
Product NDC 21130-519
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen
Dosage Form Name CAPSULE, LIQUID FILLED
Route Name ORAL
Start Marketing Date 20040510
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Safeway
Substance Name ACETAMINOPHEN
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Rapid Release Pain Reliever


General Information