Package 71205-647-90

Brand: meclizine hydrochloride

Generic: meclizine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71205-647-90
Digits Only 7120564790
Product NDC 71205-647
Description

90 TABLET in 1 BOTTLE (71205-647-90)

Marketing

Marketing Status
Marketed Since 2022-03-23
Brand meclizine hydrochloride
Generic meclizine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "bf1db485-1415-4229-b3e1-05a6f62ff7dd", "openfda": {"upc": ["0371205647902"], "unii": ["HDP7W44CIO"], "rxcui": ["995624"], "spl_set_id": ["92e8390b-5173-4aa1-906d-35d2c0eaaaf6"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "10 TABLET in 1 BOTTLE (71205-647-10)", "package_ndc": "71205-647-10", "marketing_start_date": "20220323"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71205-647-90)", "package_ndc": "71205-647-90", "marketing_start_date": "20220323"}], "brand_name": "Meclizine Hydrochloride", "product_id": "71205-647_bf1db485-1415-4229-b3e1-05a6f62ff7dd", "dosage_form": "TABLET", "pharm_class": ["Antiemetic [EPC]", "Emesis Suppression [PE]"], "product_ndc": "71205-647", "generic_name": "Meclizine Hydrochloride", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Meclizine Hydrochloride", "active_ingredients": [{"name": "MECLIZINE HYDROCHLORIDE", "strength": "12.5 mg/1"}], "application_number": "NDA010721", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20200115", "listing_expiration_date": "20261231"}