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sunmark nasal decongestant pe - 49348-700-07 - (Phenylephrine Hydrochloride)

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Drug Information of sunmark nasal decongestant pe

Product NDC: 49348-700
Proprietary Name: sunmark nasal decongestant pe
Non Proprietary Name: Phenylephrine Hydrochloride
Active Ingredient(s): 10    mg/1 & nbsp;   Phenylephrine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of sunmark nasal decongestant pe

Product NDC: 49348-700
Labeler Name: McKesson
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20050214

Package Information of sunmark nasal decongestant pe

Package NDC: 49348-700-07
Package Description: 2 BLISTER PACK in 1 CARTON (49348-700-07) > 18 TABLET in 1 BLISTER PACK

NDC Information of sunmark nasal decongestant pe

NDC Code 49348-700-07
Proprietary Name sunmark nasal decongestant pe
Package Description 2 BLISTER PACK in 1 CARTON (49348-700-07) > 18 TABLET in 1 BLISTER PACK
Product NDC 49348-700
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Phenylephrine Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20050214
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name McKesson
Substance Name PHENYLEPHRINE HYDROCHLORIDE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of sunmark nasal decongestant pe


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