Package 37808-903-12

Brand: motion sickness

Generic: meclizine hcl
NDC Package

Package Facts

Identity

Package NDC 37808-903-12
Digits Only 3780890312
Product NDC 37808-903
Product ID 37808-903_3473b0b6-6443-4b2d-b8b1-89350fc754ad
Description

100 TABLET in 1 BOTTLE (37808-903-12)

Marketing

Marketing Status
Marketed Since 2019-06-24
Brand motion sickness
Generic meclizine hcl
Sample Package No

Linked Drug Pages (1)

Motion Sickness ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3473b0b6-6443-4b2d-b8b1-89350fc754ad", "openfda": {"upc": ["0041220834723"], "unii": ["HDP7W44CIO"], "rxcui": ["995666"], "spl_set_id": ["9837e9af-c542-4c0f-be33-94927d67c6a7"], "manufacturer_name": ["H E B"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (37808-903-12)", "package_ndc": "37808-903-12", "marketing_start_date": "20190624"}], "brand_name": "Motion Sickness", "product_id": "37808-903_3473b0b6-6443-4b2d-b8b1-89350fc754ad", "dosage_form": "TABLET", "pharm_class": ["Antiemetic [EPC]", "Emesis Suppression [PE]"], "product_ndc": "37808-903", "generic_name": "Meclizine HCl", "labeler_name": "H E B", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Motion Sickness", "active_ingredients": [{"name": "MECLIZINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "M009", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20190624", "listing_expiration_date": "20261231"}