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OXYMETAZOLINE HYDROCHLORIDE - 21695-875-30 - (OXYMETAZOLINE HYDROCHLORIDE)

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Drug Information of OXYMETAZOLINE HYDROCHLORIDE

Product NDC: 21695-875
Proprietary Name: OXYMETAZOLINE HYDROCHLORIDE
Non Proprietary Name: OXYMETAZOLINE HYDROCHLORIDE
Active Ingredient(s): .5    mg/mL & nbsp;   OXYMETAZOLINE HYDROCHLORIDE
Administration Route(s): NASAL
Dosage Form(s): SPRAY, METERED
Coding System: National Drug Codes(NDC)

Labeler Information of OXYMETAZOLINE HYDROCHLORIDE

Product NDC: 21695-875
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20081211

Package Information of OXYMETAZOLINE HYDROCHLORIDE

Package NDC: 21695-875-30
Package Description: 30 mL in 1 BOTTLE, SPRAY (21695-875-30)

NDC Information of OXYMETAZOLINE HYDROCHLORIDE

NDC Code 21695-875-30
Proprietary Name OXYMETAZOLINE HYDROCHLORIDE
Package Description 30 mL in 1 BOTTLE, SPRAY (21695-875-30)
Product NDC 21695-875
Product Type Name HUMAN OTC DRUG
Non Proprietary Name OXYMETAZOLINE HYDROCHLORIDE
Dosage Form Name SPRAY, METERED
Route Name NASAL
Start Marketing Date 20081211
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Rebel Distributors Corp
Substance Name OXYMETAZOLINE HYDROCHLORIDE
Strength Number .5
Strength Unit mg/mL
Pharmaceutical Classes

Complete Information of OXYMETAZOLINE HYDROCHLORIDE


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