ACEPHEN - 0713-0165-01 - (Acetaminophen)

Alphabetical Index

Drug Information of ACEPHEN

Product NDC: 0713-0165
Proprietary Name: ACEPHEN
Non Proprietary Name: Acetaminophen
Active Ingredient(s): 650    mg/1 & nbsp;   Acetaminophen
Administration Route(s): RECTAL
Dosage Form(s): SUPPOSITORY
Coding System: National Drug Codes(NDC)

Labeler Information of ACEPHEN

Product NDC: 0713-0165
Labeler Name: G&W Laboratories, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA072237
Marketing Category: ANDA
Start Marketing Date: 19920327

Package Information of ACEPHEN

Package NDC: 0713-0165-01
Package Description: 100 SUPPOSITORY in 1 BOX (0713-0165-01)

NDC Information of ACEPHEN

NDC Code 0713-0165-01
Proprietary Name ACEPHEN
Package Description 100 SUPPOSITORY in 1 BOX (0713-0165-01)
Product NDC 0713-0165
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen
Dosage Form Name SUPPOSITORY
Route Name RECTAL
Start Marketing Date 19920327
Marketing Category Name ANDA
Labeler Name G&W Laboratories, Inc.
Strength Number 650
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of ACEPHEN

General Information