Package 76420-130-30

Brand: meclizine hydrochloride

Generic: meclizine hydrocloride
NDC Package

Package Facts

Identity

Package NDC 76420-130-30
Digits Only 7642013030
Product NDC 76420-130
Description

30 TABLET in 1 BOTTLE (76420-130-30)

Marketing

Marketing Status
Marketed Since 2020-10-30
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": "b2ddcdd0-726a-99df-e053-2a95a90a8818", "openfda": {"unii": ["HDP7W44CIO"], "rxcui": ["995666"], "spl_set_id": ["5c70e61b-a1e6-4981-92e2-1050cee08baa"], "manufacturer_name": ["Asclemed USA, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "10 TABLET in 1 BOTTLE (76420-130-10)", "package_ndc": "76420-130-10", "marketing_start_date": "20201030"}, {"sample": false, "description": "20 TABLET in 1 BOTTLE (76420-130-20)", "package_ndc": "76420-130-20", "marketing_start_date": "20201030"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (76420-130-30)", "package_ndc": "76420-130-30", "marketing_start_date": "20201030"}], "brand_name": "MECLIZINE HYDROCHLORIDE", "product_id": "76420-130_b2ddcdd0-726a-99df-e053-2a95a90a8818", "dosage_form": "TABLET", "pharm_class": ["Antiemetic [EPC]", "Emesis Suppression [PE]"], "product_ndc": "76420-130", "generic_name": "Meclizine Hydrocloride", "labeler_name": "Asclemed USA, Inc.", "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": "20100604", "listing_expiration_date": "20261231"}