Package 71335-2451-2
Brand: hydroxyzine hydrochloride
Generic: hydroxyzine hydrochloridePackage Facts
Identity
Package NDC
71335-2451-2
Digits Only
7133524512
Product NDC
71335-2451
Description
60 TABLET, FILM COATED in 1 BOTTLE (71335-2451-2)
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": "897a39b6-65b1-4e52-85e9-2650d23a4dc0", "openfda": {"unii": ["76755771U3"], "rxcui": ["995258"], "spl_set_id": ["3f5be725-8ade-4889-b6b1-7d45f5458546"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71335-2451-1)", "package_ndc": "71335-2451-1", "marketing_start_date": "20240820"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71335-2451-2)", "package_ndc": "71335-2451-2", "marketing_start_date": "20240820"}, {"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (71335-2451-3)", "package_ndc": "71335-2451-3", "marketing_start_date": "20240820"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (71335-2451-4)", "package_ndc": "71335-2451-4", "marketing_start_date": "20240820"}, {"sample": false, "description": "15 TABLET, FILM COATED in 1 BOTTLE (71335-2451-5)", "package_ndc": "71335-2451-5", "marketing_start_date": "20240820"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71335-2451-6)", "package_ndc": "71335-2451-6", "marketing_start_date": "20240820"}, {"sample": false, "description": "19 TABLET, FILM COATED in 1 BOTTLE (71335-2451-7)", "package_ndc": "71335-2451-7", "marketing_start_date": "20240820"}, {"sample": false, "description": "10 TABLET, FILM COATED in 1 BOTTLE (71335-2451-8)", "package_ndc": "71335-2451-8", "marketing_start_date": "20240820"}], "brand_name": "Hydroxyzine Hydrochloride", "product_id": "71335-2451_897a39b6-65b1-4e52-85e9-2650d23a4dc0", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antihistamine [EPC]", "Histamine Receptor Antagonists [MoA]"], "product_ndc": "71335-2451", "generic_name": "Hydroxyzine Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydroxyzine Hydrochloride", "active_ingredients": [{"name": "HYDROXYZINE DIHYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "ANDA040786", "marketing_category": "ANDA", "marketing_start_date": "20120724", "listing_expiration_date": "20261231"}