Package 60760-087-90

Brand: meclizine hydrochloride

Generic: meclizine hydrocloride
NDC Package

Package Facts

Identity

Package NDC 60760-087-90
Digits Only 6076008790
Product NDC 60760-087
Description

90 TABLET in 1 BOTTLE, PLASTIC (60760-087-90)

Marketing

Marketing Status
Marketed Since 2019-04-18
Brand meclizine hydrochloride
Generic meclizine hydrocloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "ef545c37-addf-340f-e053-2995a90aad16", "openfda": {"unii": ["HDP7W44CIO"], "rxcui": ["995666"], "spl_set_id": ["87210edf-0bf9-2577-e053-2991aa0aaceb"], "manufacturer_name": ["St. Mary's Medical Park Pharmacy"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (60760-087-90)", "package_ndc": "60760-087-90", "marketing_start_date": "20190418"}], "brand_name": "MECLIZINE HYDROCHLORIDE", "product_id": "60760-087_ef545c37-addf-340f-e053-2995a90aad16", "dosage_form": "TABLET", "pharm_class": ["Antiemetic [EPC]", "Emesis Suppression [PE]"], "product_ndc": "60760-087", "generic_name": "Meclizine Hydrocloride", "labeler_name": "St. Mary's Medical Park Pharmacy", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "MECLIZINE HYDROCHLORIDE", "active_ingredients": [{"name": "MECLIZINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "ANDA040659", "marketing_category": "ANDA", "marketing_start_date": "20190418", "listing_expiration_date": "20261231"}