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Phenylephrine Hydrochloride - 17478-200-20 - (Phenylephrine Hydrochloride)

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Drug Information of Phenylephrine Hydrochloride

Product NDC: 17478-200
Proprietary Name: Phenylephrine Hydrochloride
Non Proprietary Name: Phenylephrine Hydrochloride
Active Ingredient(s): 25    mg/mL & nbsp;   Phenylephrine Hydrochloride
Administration Route(s): OPHTHALMIC
Dosage Form(s): SOLUTION/ DROPS
Coding System: National Drug Codes(NDC)

Labeler Information of Phenylephrine Hydrochloride

Product NDC: 17478-200
Labeler Name: Akorn, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 19910701

Package Information of Phenylephrine Hydrochloride

Package NDC: 17478-200-20
Package Description: 1 BOTTLE, DROPPER in 1 CARTON (17478-200-20) > 2 mL in 1 BOTTLE, DROPPER

NDC Information of Phenylephrine Hydrochloride

NDC Code 17478-200-20
Proprietary Name Phenylephrine Hydrochloride
Package Description 1 BOTTLE, DROPPER in 1 CARTON (17478-200-20) > 2 mL in 1 BOTTLE, DROPPER
Product NDC 17478-200
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Phenylephrine Hydrochloride
Dosage Form Name SOLUTION/ DROPS
Route Name OPHTHALMIC
Start Marketing Date 19910701
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name Akorn, Inc.
Substance Name PHENYLEPHRINE HYDROCHLORIDE
Strength Number 25
Strength Unit mg/mL
Pharmaceutical Classes

Complete Information of Phenylephrine Hydrochloride


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