Package 42708-102-30

Brand: meclizine hydrocloride

Generic: meclizine hydrocloride
NDC Package Sample

Package Facts

Identity

Package NDC 42708-102-30
Digits Only 4270810230
Product NDC 42708-102
Product ID 42708-102_459c95f7-ca90-7ded-e063-6394a90a0530
Description

30 TABLET in 1 BOTTLE (42708-102-30)

Marketing

Marketing Status
Discontinued 2026-10-31
Brand meclizine hydrocloride
Generic meclizine hydrocloride
Sample Package Yes

Linked Drug Pages (1)

Meclizine Hydrocloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "459c95f7-ca90-7ded-e063-6394a90a0530", "openfda": {"unii": ["HDP7W44CIO"], "rxcui": ["995666"], "spl_set_id": ["aa0fb895-a867-4482-9bc2-16eee8bfaaa0"], "manufacturer_name": ["QPharma Inc"]}, "finished": true, "packaging": [{"sample": true, "description": "30 TABLET in 1 BOTTLE (42708-102-30)", "package_ndc": "42708-102-30", "marketing_end_date": "20261031", "marketing_start_date": "20191018"}], "brand_name": "Meclizine Hydrocloride", "product_id": "42708-102_459c95f7-ca90-7ded-e063-6394a90a0530", "dosage_form": "TABLET", "pharm_class": ["Antiemetic [EPC]", "Emesis Suppression [PE]"], "product_ndc": "42708-102", "generic_name": "Meclizine Hydrocloride", "labeler_name": "QPharma Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Meclizine Hydrocloride", "active_ingredients": [{"name": "MECLIZINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "ANDA040659", "marketing_category": "ANDA", "marketing_end_date": "20261031", "marketing_start_date": "20100604"}