Package 71335-2636-6
Brand: hydroxyzine hydrochloride
Generic: hydroxyzine hydrochloridePackage Facts
Identity
Package NDC
71335-2636-6
Digits Only
7133526366
Product NDC
71335-2636
Description
60 TABLET, FILM COATED in 1 BOTTLE (71335-2636-6)
Marketing
Marketing Status
Brand
hydroxyzine hydrochloride
Generic
hydroxyzine hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "f3f81841-db62-4a69-b56c-466088cfa950", "openfda": {"unii": ["76755771U3"], "rxcui": ["995218"], "spl_set_id": ["6577589f-1a80-41d8-847a-70c3f38d8dc0"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71335-2636-1)", "package_ndc": "71335-2636-1", "marketing_start_date": "20250602"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (71335-2636-2)", "package_ndc": "71335-2636-2", "marketing_start_date": "20250602"}, {"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (71335-2636-3)", "package_ndc": "71335-2636-3", "marketing_start_date": "20250602"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71335-2636-4)", "package_ndc": "71335-2636-4", "marketing_start_date": "20250602"}, {"sample": false, "description": "15 TABLET, FILM COATED in 1 BOTTLE (71335-2636-5)", "package_ndc": "71335-2636-5", "marketing_start_date": "20250602"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71335-2636-6)", "package_ndc": "71335-2636-6", "marketing_start_date": "20250602"}, {"sample": false, "description": "120 TABLET, FILM COATED in 1 BOTTLE (71335-2636-7)", "package_ndc": "71335-2636-7", "marketing_start_date": "20250602"}, {"sample": false, "description": "10 TABLET, FILM COATED in 1 BOTTLE (71335-2636-8)", "package_ndc": "71335-2636-8", "marketing_start_date": "20250602"}], "brand_name": "HYDROXYZINE HYDROCHLORIDE", "product_id": "71335-2636_f3f81841-db62-4a69-b56c-466088cfa950", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antihistamine [EPC]", "Histamine Receptor Antagonists [MoA]"], "product_ndc": "71335-2636", "generic_name": "hydroxyzine hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "HYDROXYZINE HYDROCHLORIDE", "active_ingredients": [{"name": "HYDROXYZINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA217652", "marketing_category": "ANDA", "marketing_start_date": "20230822", "listing_expiration_date": "20261231"}