Package 70518-3768-0

Brand: meclizine hydrochloride

Generic: meclizine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-3768-0
Digits Only 7051837680
Product NDC 70518-3768
Product ID 70518-3768_3b259db1-38f1-82a1-e063-6294a90a8ad9
Description

30 TABLET in 1 BOTTLE, PLASTIC (70518-3768-0)

Marketing

Marketing Status
Marketed Since 2023-06-19
Brand meclizine hydrochloride
Generic meclizine hydrochloride
Sample Package No

Linked Drug Pages (0)

No linked drugs yet.

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3b259db1-38f1-82a1-e063-6294a90a8ad9", "openfda": {"unii": ["HDP7W44CIO"], "rxcui": ["995624"], "spl_set_id": ["d53bf04e-5cfc-4974-9b24-2cce545d1bd0"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (70518-3768-0)", "package_ndc": "70518-3768-0", "marketing_start_date": "20230619"}], "brand_name": "Meclizine Hydrochloride", "product_id": "70518-3768_3b259db1-38f1-82a1-e063-6294a90a8ad9", "dosage_form": "TABLET", "pharm_class": ["Antiemetic [EPC]", "Emesis Suppression [PE]"], "product_ndc": "70518-3768", "generic_name": "Meclizine Hydrochloride", "labeler_name": "REMEDYREPACK INC.", "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": "20230619", "listing_expiration_date": "20261231"}