Package 24658-783-10

Brand: hydroxyzine hydrochloride

Generic: hydroxyzine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 24658-783-10
Digits Only 2465878310
Product NDC 24658-783
Product ID 24658-783_384448bf-baa4-482b-91cd-585b03c62907
Description

1000 TABLET, FILM COATED in 1 BOTTLE (24658-783-10)

Marketing

Marketing Status
Marketed Since 2021-07-21
Brand hydroxyzine hydrochloride
Generic hydroxyzine hydrochloride
Sample Package No

Linked Drug Pages (1)

Hydroxyzine Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "384448bf-baa4-482b-91cd-585b03c62907", "openfda": {"upc": ["0324658782102", "0324658781105", "0324658783109"], "unii": ["76755771U3"], "rxcui": ["995218", "995258", "995281"], "spl_set_id": ["19fe26a9-eb1a-4c5b-a5e4-65223ee56ad1"], "manufacturer_name": ["PURACAP LABORATORIES LLC DBA BLU PHARMACEUTICALS"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (24658-783-10)", "package_ndc": "24658-783-10", "marketing_start_date": "20210721"}], "brand_name": "Hydroxyzine Hydrochloride", "product_id": "24658-783_384448bf-baa4-482b-91cd-585b03c62907", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antihistamine [EPC]", "Histamine Receptor Antagonists [MoA]"], "product_ndc": "24658-783", "generic_name": "Hydroxyzine Hydrochloride", "labeler_name": "PURACAP LABORATORIES LLC DBA BLU PHARMACEUTICALS", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydroxyzine Hydrochloride", "active_ingredients": [{"name": "HYDROXYZINE DIHYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA040604", "marketing_category": "ANDA", "marketing_start_date": "20210721", "listing_expiration_date": "20271231"}