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Suphedrine PE - 70253-453-07 - (Phenylephrine HCl)

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Drug Information of Suphedrine PE

Product NDC: 70253-453
Proprietary Name: Suphedrine PE
Non Proprietary Name: Phenylephrine HCl
Active Ingredient(s): 10    mg/1 & nbsp;   Phenylephrine HCl
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Suphedrine PE

Product NDC: 70253-453
Labeler Name: NASH-FINCH COMPANY
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20041206

Package Information of Suphedrine PE

Package NDC: 70253-453-07
Package Description: 1 BLISTER PACK in 1 CARTON (70253-453-07) > 36 TABLET, FILM COATED in 1 BLISTER PACK

NDC Information of Suphedrine PE

NDC Code 70253-453-07
Proprietary Name Suphedrine PE
Package Description 1 BLISTER PACK in 1 CARTON (70253-453-07) > 36 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC 70253-453
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Phenylephrine HCl
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20041206
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name NASH-FINCH COMPANY
Substance Name PHENYLEPHRINE HYDROCHLORIDE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Suphedrine PE


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