Package 59651-808-01

Brand: meclizine hydrochloride

Generic: meclizine
NDC Package

Package Facts

Identity

Package NDC 59651-808-01
Digits Only 5965180801
Product NDC 59651-808
Product ID 59651-808_beb3c7f2-c0f4-41d9-a903-63a6847e0997
Description

100 TABLET in 1 BOTTLE (59651-808-01)

Marketing

Marketing Status
Marketed Since 2023-09-14
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": "beb3c7f2-c0f4-41d9-a903-63a6847e0997", "openfda": {"unii": ["HDP7W44CIO"], "rxcui": ["995624", "995666", "995686"], "spl_set_id": ["beb3c7f2-c0f4-41d9-a903-63a6847e0997"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (59651-808-01)", "package_ndc": "59651-808-01", "marketing_start_date": "20230914"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (59651-808-99)", "package_ndc": "59651-808-99", "marketing_start_date": "20230914"}], "brand_name": "MECLIZINE HYDROCHLORIDE", "product_id": "59651-808_beb3c7f2-c0f4-41d9-a903-63a6847e0997", "dosage_form": "TABLET", "pharm_class": ["Antiemetic [EPC]", "Emesis Suppression [PE]"], "product_ndc": "59651-808", "generic_name": "MECLIZINE", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "MECLIZINE HYDROCHLORIDE", "active_ingredients": [{"name": "MECLIZINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "ANDA202640", "marketing_category": "ANDA", "marketing_start_date": "20230914", "listing_expiration_date": "20261231"}