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RHINOFLEX-650 - 15370-650-10 - (Acetaminophen and Phenyltoloxamine Citrate)

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Drug Information of RHINOFLEX-650

Product NDC: 15370-650
Proprietary Name: RHINOFLEX-650
Non Proprietary Name: Acetaminophen and Phenyltoloxamine Citrate
Active Ingredient(s): 650; 50    mg/1; mg/1 & nbsp;   Acetaminophen and Phenyltoloxamine Citrate
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of RHINOFLEX-650

Product NDC: 15370-650
Labeler Name: CARWIN ASSOCIATES, INC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20000131

Package Information of RHINOFLEX-650

Package NDC: 15370-650-10
Package Description: 100 TABLET in 1 BOTTLE (15370-650-10)

NDC Information of RHINOFLEX-650

NDC Code 15370-650-10
Proprietary Name RHINOFLEX-650
Package Description 100 TABLET in 1 BOTTLE (15370-650-10)
Product NDC 15370-650
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Acetaminophen and Phenyltoloxamine Citrate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20000131
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name CARWIN ASSOCIATES, INC
Substance Name ACETAMINOPHEN; PHENYLTOLOXAMINE CITRATE
Strength Number 650; 50
Strength Unit mg/1; mg/1
Pharmaceutical Classes

Complete Information of RHINOFLEX-650


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