Package 60760-285-20

Brand: hydroxyzine hydrochloride

Generic: hydroxyzine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 60760-285-20
Digits Only 6076028520
Product NDC 60760-285
Product ID 60760-285_4537cfd9-9816-831c-e063-6394a90a86f9
Description

20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-285-20)

Marketing

Marketing Status
Marketed Since 2020-02-19
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": "4537cfd9-9816-831c-e063-6394a90a86f9", "openfda": {"unii": ["76755771U3"], "rxcui": ["995218"], "spl_set_id": ["9ef6a4b7-362d-61b4-e053-2995a90a0ebb"], "manufacturer_name": ["St Mary's Medical Park Pharmacy"]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-285-20)", "package_ndc": "60760-285-20", "marketing_start_date": "20200219"}], "brand_name": "Hydroxyzine Hydrochloride", "product_id": "60760-285_4537cfd9-9816-831c-e063-6394a90a86f9", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antihistamine [EPC]", "Histamine Receptor Antagonists [MoA]"], "product_ndc": "60760-285", "generic_name": "Hydroxyzine Hydrochloride", "labeler_name": "St Mary's Medical Park Pharmacy", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydroxyzine Hydrochloride", "active_ingredients": [{"name": "HYDROXYZINE DIHYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA088617", "marketing_category": "ANDA", "marketing_start_date": "20200219", "listing_expiration_date": "20261231"}