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ACETAMINOPHEN SINUS CONGESTION AND PAIN - 46084-101-30 - (ACETAMINOPHEN, PHENYLEPHRINE HYDROCHLORIDE)

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Drug Information of ACETAMINOPHEN SINUS CONGESTION AND PAIN

Product NDC: 46084-101
Proprietary Name: ACETAMINOPHEN SINUS CONGESTION AND PAIN
Non Proprietary Name: ACETAMINOPHEN, PHENYLEPHRINE HYDROCHLORIDE
Active Ingredient(s): 325; 5    mg/1; mg/1 & nbsp;   ACETAMINOPHEN, PHENYLEPHRINE HYDROCHLORIDE
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of ACETAMINOPHEN SINUS CONGESTION AND PAIN

Product NDC: 46084-101
Labeler Name: A P J Laboratories Limited
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20130606

Package Information of ACETAMINOPHEN SINUS CONGESTION AND PAIN

Package NDC: 46084-101-30
Package Description: 30 TABLET in 1 BLISTER PACK (46084-101-30)

NDC Information of ACETAMINOPHEN SINUS CONGESTION AND PAIN

NDC Code 46084-101-30
Proprietary Name ACETAMINOPHEN SINUS CONGESTION AND PAIN
Package Description 30 TABLET in 1 BLISTER PACK (46084-101-30)
Product NDC 46084-101
Product Type Name HUMAN OTC DRUG
Non Proprietary Name ACETAMINOPHEN, PHENYLEPHRINE HYDROCHLORIDE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130606
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name A P J Laboratories Limited
Substance Name ACETAMINOPHEN; PHENYLEPHRINE HYDROCHLORIDE
Strength Number 325; 5
Strength Unit mg/1; mg/1
Pharmaceutical Classes

Complete Information of ACETAMINOPHEN SINUS CONGESTION AND PAIN


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