ACEPHEN - 0713-0118-50 - (Acetaminophen)

Alphabetical Index


Drug Information of ACEPHEN

Product NDC: 0713-0118
Proprietary Name: ACEPHEN
Non Proprietary Name: Acetaminophen
Active Ingredient(s): 120    mg/1 & nbsp;   Acetaminophen
Administration Route(s): RECTAL
Dosage Form(s): SUPPOSITORY
Coding System: National Drug Codes(NDC)

Labeler Information of ACEPHEN

Product NDC: 0713-0118
Labeler Name: G&W Laboratories, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: NDA018060
Marketing Category: NDA
Start Marketing Date: 19820101

Package Information of ACEPHEN

Package NDC: 0713-0118-50
Package Description: 50 SUPPOSITORY in 1 BOX (0713-0118-50)

NDC Information of ACEPHEN

NDC Code 0713-0118-50
Proprietary Name ACEPHEN
Package Description 50 SUPPOSITORY in 1 BOX (0713-0118-50)
Product NDC 0713-0118
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen
Dosage Form Name SUPPOSITORY
Route Name RECTAL
Start Marketing Date 19820101
Marketing Category Name NDA
Labeler Name G&W Laboratories, Inc.
Substance Name ACETAMINOPHEN
Strength Number 120
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of ACEPHEN


General Information