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Acetaminophen, Phenylephrine Hydrochloride - 57344-120-03 - (ACETAMINOPHEN and PHENYLEPHRINE HYDROCHLORIDE)

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Drug Information of Acetaminophen, Phenylephrine Hydrochloride

Product NDC: 57344-120
Proprietary Name: Acetaminophen, Phenylephrine Hydrochloride
Non Proprietary Name: ACETAMINOPHEN and PHENYLEPHRINE HYDROCHLORIDE
Active Ingredient(s): 325; 5    mg/1; mg/1 & nbsp;   ACETAMINOPHEN and PHENYLEPHRINE HYDROCHLORIDE
Administration Route(s): ORAL
Dosage Form(s): TABLET, COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Acetaminophen, Phenylephrine Hydrochloride

Product NDC: 57344-120
Labeler Name: AAA Pharmaceutical, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20121222

Package Information of Acetaminophen, Phenylephrine Hydrochloride

Package NDC: 57344-120-03
Package Description: 4 BLISTER PACK in 1 CARTON (57344-120-03) > 12 TABLET, COATED in 1 BLISTER PACK

NDC Information of Acetaminophen, Phenylephrine Hydrochloride

NDC Code 57344-120-03
Proprietary Name Acetaminophen, Phenylephrine Hydrochloride
Package Description 4 BLISTER PACK in 1 CARTON (57344-120-03) > 12 TABLET, COATED in 1 BLISTER PACK
Product NDC 57344-120
Product Type Name HUMAN OTC DRUG
Non Proprietary Name ACETAMINOPHEN and PHENYLEPHRINE HYDROCHLORIDE
Dosage Form Name TABLET, COATED
Route Name ORAL
Start Marketing Date 20121222
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name AAA Pharmaceutical, Inc.
Substance Name ACETAMINOPHEN; PHENYLEPHRINE HYDROCHLORIDE
Strength Number 325; 5
Strength Unit mg/1; mg/1
Pharmaceutical Classes

Complete Information of Acetaminophen, Phenylephrine Hydrochloride


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