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Sudogest PE - 0904-5733-62 - (Phenylephrine HCl)

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Drug Information of Sudogest PE

Product NDC: 0904-5733
Proprietary Name: Sudogest 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 Sudogest PE

Product NDC: 0904-5733
Labeler Name: Major Pharmaceuticals
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20041206

Package Information of Sudogest PE

Package NDC: 0904-5733-62
Package Description: 1 BLISTER PACK in 1 CARTON (0904-5733-62) > 72 TABLET, FILM COATED in 1 BLISTER PACK

NDC Information of Sudogest PE

NDC Code 0904-5733-62
Proprietary Name Sudogest PE
Package Description 1 BLISTER PACK in 1 CARTON (0904-5733-62) > 72 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC 0904-5733
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 Major Pharmaceuticals
Substance Name PHENYLEPHRINE HYDROCHLORIDE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Sudogest PE


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