Package 37808-004-10

Brand: nasal

Generic: oxymetazoline hydrochloride
NDC Package

Package Facts

Identity

Package NDC 37808-004-10
Digits Only 3780800410
Product NDC 37808-004
Product ID 37808-004_91fa3ae3-b502-4320-8167-68893aa41e6d
Description

1 BOTTLE, SPRAY in 1 CARTON (37808-004-10) / 30 mL in 1 BOTTLE, SPRAY

Marketing

Marketing Status
Marketed Since 2014-12-02
Brand nasal
Generic oxymetazoline hydrochloride
Sample Package No

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Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["NASAL"], "spl_id": "91fa3ae3-b502-4320-8167-68893aa41e6d", "openfda": {"unii": ["K89MJ0S5VY"], "rxcui": ["1000990"], "spl_set_id": ["3c301993-642a-487c-96a2-ebc4ef90dc88"], "manufacturer_name": ["H E B"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, SPRAY in 1 CARTON (37808-004-10)  / 30 mL in 1 BOTTLE, SPRAY", "package_ndc": "37808-004-10", "marketing_start_date": "20141202"}], "brand_name": "nasal", "product_id": "37808-004_91fa3ae3-b502-4320-8167-68893aa41e6d", "dosage_form": "SPRAY", "pharm_class": ["Imidazolines [CS]", "Increased Sympathetic Activity [PE]", "Vasoconstriction [PE]", "Vasoconstrictor [EPC]"], "product_ndc": "37808-004", "generic_name": "oxymetazoline hydrochloride", "labeler_name": "H E B", "product_type": "HUMAN OTC DRUG", "brand_name_base": "nasal", "active_ingredients": [{"name": "OXYMETAZOLINE HYDROCHLORIDE", "strength": ".05 g/100mL"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20141202", "listing_expiration_date": "20261231"}