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OXYMETAZOLINE HYDROCHLORIDE - 65841-711-07 - (OXYMETAZOLINE HYDROCHLORIDE)

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Drug Information of OXYMETAZOLINE HYDROCHLORIDE

Product NDC: 65841-711
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: 65841-711
Labeler Name: Cadila Healthcare Limited
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20090924

Package Information of OXYMETAZOLINE HYDROCHLORIDE

Package NDC: 65841-711-07
Package Description: 1 INHALER in 1 CARTON (65841-711-07) > 22 mL in 1 INHALER

NDC Information of OXYMETAZOLINE HYDROCHLORIDE

NDC Code 65841-711-07
Proprietary Name OXYMETAZOLINE HYDROCHLORIDE
Package Description 1 INHALER in 1 CARTON (65841-711-07) > 22 mL in 1 INHALER
Product NDC 65841-711
Product Type Name HUMAN OTC DRUG
Non Proprietary Name OXYMETAZOLINE HYDROCHLORIDE
Dosage Form Name SPRAY, METERED
Route Name NASAL
Start Marketing Date 20090924
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Cadila Healthcare Limited
Substance Name OXYMETAZOLINE HYDROCHLORIDE
Strength Number .5
Strength Unit mg/mL
Pharmaceutical Classes

Complete Information of OXYMETAZOLINE HYDROCHLORIDE


General Information