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Oxymetazoline Hydrochloride - 51672-2030-5 - (Oxymetazoline Hydrochloride)

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Drug Information of Oxymetazoline Hydrochloride

Product NDC: 51672-2030
Proprietary Name: Oxymetazoline Hydrochloride
Non Proprietary Name: Oxymetazoline Hydrochloride
Active Ingredient(s): .05    g/100mL & nbsp;   Oxymetazoline Hydrochloride
Administration Route(s): NASAL
Dosage Form(s): SPRAY
Coding System: National Drug Codes(NDC)

Labeler Information of Oxymetazoline Hydrochloride

Product NDC: 51672-2030
Labeler Name: Taro Pharmaceuticals U.S.A., Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20060225

Package Information of Oxymetazoline Hydrochloride

Package NDC: 51672-2030-5
Package Description: 1 BOTTLE, SPRAY in 1 CARTON (51672-2030-5) > 15 mL in 1 BOTTLE, SPRAY

NDC Information of Oxymetazoline Hydrochloride

NDC Code 51672-2030-5
Proprietary Name Oxymetazoline Hydrochloride
Package Description 1 BOTTLE, SPRAY in 1 CARTON (51672-2030-5) > 15 mL in 1 BOTTLE, SPRAY
Product NDC 51672-2030
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Oxymetazoline Hydrochloride
Dosage Form Name SPRAY
Route Name NASAL
Start Marketing Date 20060225
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Taro Pharmaceuticals U.S.A., Inc.
Substance Name OXYMETAZOLINE HYDROCHLORIDE
Strength Number .05
Strength Unit g/100mL
Pharmaceutical Classes

Complete Information of Oxymetazoline Hydrochloride


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