Package 68788-8633-3

Brand: meclizine hydrochloride

Generic: meclizine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68788-8633-3
Digits Only 6878886333
Product NDC 68788-8633
Product ID 68788-8633_769c5aef-cef1-4cd7-a775-3facb91cc01f
Description

30 TABLET in 1 BOTTLE (68788-8633-3)

Marketing

Marketing Status
Marketed Since 2024-04-16
Brand meclizine hydrochloride
Generic meclizine hydrochloride
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": "769c5aef-cef1-4cd7-a775-3facb91cc01f", "openfda": {"unii": ["HDP7W44CIO"], "rxcui": ["995624"], "spl_set_id": ["d7d31433-8f39-4fe6-b542-1b4410122db7"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "10 TABLET in 1 BOTTLE (68788-8633-1)", "package_ndc": "68788-8633-1", "marketing_start_date": "20240416"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (68788-8633-3)", "package_ndc": "68788-8633-3", "marketing_start_date": "20240416"}], "brand_name": "Meclizine Hydrochloride", "product_id": "68788-8633_769c5aef-cef1-4cd7-a775-3facb91cc01f", "dosage_form": "TABLET", "pharm_class": ["Antiemetic [EPC]", "Emesis Suppression [PE]"], "product_ndc": "68788-8633", "generic_name": "Meclizine Hydrochloride", "labeler_name": "Preferred Pharmaceuticals 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": "20240416", "listing_expiration_date": "20261231"}