Package 0615-8514-39

Brand: meclizine hydrochloride

Generic: meclizine
NDC Package

Package Facts

Identity

Package NDC 0615-8514-39
Digits Only 0615851439
Product NDC 0615-8514
Product ID 0615-8514_7c702061-6604-4b46-b035-dd0fb4d25165
Description

30 TABLET in 1 BLISTER PACK (0615-8514-39)

Marketing

Marketing Status
Marketed Since 2024-07-15
Brand meclizine hydrochloride
Generic meclizine
Sample Package No

Linked Drug Pages (1)

MECLIZINE HYDROCHLORIDE ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "7c702061-6604-4b46-b035-dd0fb4d25165", "openfda": {"unii": ["HDP7W44CIO"], "rxcui": ["995624", "995666"], "spl_set_id": ["1a33dec1-8d59-48bd-aaef-77d162194d57"], "manufacturer_name": ["NCS HealthCare of KY, LLC dba Vangard Labs"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (0615-8514-39)", "package_ndc": "0615-8514-39", "marketing_start_date": "20240715"}], "brand_name": "MECLIZINE HYDROCHLORIDE", "product_id": "0615-8514_7c702061-6604-4b46-b035-dd0fb4d25165", "dosage_form": "TABLET", "pharm_class": ["Antiemetic [EPC]", "Emesis Suppression [PE]"], "product_ndc": "0615-8514", "generic_name": "MECLIZINE", "labeler_name": "NCS HealthCare of KY, LLC dba Vangard Labs", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "MECLIZINE HYDROCHLORIDE", "active_ingredients": [{"name": "MECLIZINE HYDROCHLORIDE", "strength": "12.5 mg/1"}], "application_number": "ANDA202640", "marketing_category": "ANDA", "marketing_start_date": "20230914", "listing_expiration_date": "20261231"}