Package 0363-5172-07

Brand: meclizine hydrochloride

Generic: meclizine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0363-5172-07
Digits Only 0363517207
Product NDC 0363-5172
Product ID 0363-5172_30139dc7-2c78-271f-e063-6294a90aa001
Description

1 BLISTER PACK in 1 CARTON (0363-5172-07) / 12 TABLET, CHEWABLE in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2023-03-22
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": "30139dc7-2c78-271f-e063-6294a90aa001", "openfda": {"unii": ["HDP7W44CIO"], "rxcui": ["995632"], "spl_set_id": ["ecf8d05e-0e77-f3e8-e053-2a95a90a6604"], "manufacturer_name": ["Walgreen Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (0363-5172-07)  / 12 TABLET, CHEWABLE in 1 BLISTER PACK", "package_ndc": "0363-5172-07", "marketing_start_date": "20230322"}], "brand_name": "Meclizine Hydrochloride", "product_id": "0363-5172_30139dc7-2c78-271f-e063-6294a90aa001", "dosage_form": "TABLET, CHEWABLE", "pharm_class": ["Antiemetic [EPC]", "Emesis Suppression [PE]"], "product_ndc": "0363-5172", "generic_name": "Meclizine Hydrochloride", "labeler_name": "Walgreen Company", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Meclizine Hydrochloride", "active_ingredients": [{"name": "MECLIZINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "M009", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20230322", "listing_expiration_date": "20261231"}