Package 63029-505-16

Brand: sominex max

Generic: diphenhydramine hcl
NDC Package

Package Facts

Identity

Package NDC 63029-505-16
Digits Only 6302950516
Product NDC 63029-505
Description

1 BLISTER PACK in 1 BOX (63029-505-16) / 16 TABLET in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2012-06-01
Brand sominex max
Generic diphenhydramine hcl
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "dc571463-dbec-4984-ad42-51732470104e", "openfda": {"unii": ["TC2D6JAD40"], "rxcui": ["1085945", "1086857"], "spl_set_id": ["e8f6991f-c47a-4d12-934b-04fdf092dac3"], "manufacturer_name": ["Medtech Products Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 BOX (63029-505-16)  / 16 TABLET in 1 BLISTER PACK", "package_ndc": "63029-505-16", "marketing_start_date": "20120601"}], "brand_name": "Sominex Max", "product_id": "63029-505_dc571463-dbec-4984-ad42-51732470104e", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "63029-505", "generic_name": "Diphenhydramine HCl", "labeler_name": "Medtech Products Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Sominex Max", "active_ingredients": [{"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "M010", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20120601", "listing_expiration_date": "20261231"}