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Acetaminophen - 54868-3267-0 - (Acetaminophen)

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Drug Information of Acetaminophen

Product NDC: 54868-3267
Proprietary Name: Acetaminophen
Non Proprietary Name: Acetaminophen
Active Ingredient(s): 80    mg/.8mL & nbsp;   Acetaminophen
Administration Route(s): ORAL
Dosage Form(s): SUSPENSION/ DROPS
Coding System: National Drug Codes(NDC)

Labeler Information of Acetaminophen

Product NDC: 54868-3267
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part343
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 19940513

Package Information of Acetaminophen

Package NDC: 54868-3267-0
Package Description: 1 BOTTLE, DROPPER in 1 CARTON (54868-3267-0) > 15 mL in 1 BOTTLE, DROPPER

NDC Information of Acetaminophen

NDC Code 54868-3267-0
Proprietary Name Acetaminophen
Package Description 1 BOTTLE, DROPPER in 1 CARTON (54868-3267-0) > 15 mL in 1 BOTTLE, DROPPER
Product NDC 54868-3267
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen
Dosage Form Name SUSPENSION/ DROPS
Route Name ORAL
Start Marketing Date 19940513
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Physicians Total Care, Inc.
Substance Name ACETAMINOPHEN
Strength Number 80
Strength Unit mg/.8mL
Pharmaceutical Classes

Complete Information of Acetaminophen


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