Package 67751-221-01

Brand: sominex

Generic: diphenhydramine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 67751-221-01
Digits Only 6775122101
Product NDC 67751-221
Product ID 67751-221_2396151b-13a0-cc41-e063-6394a90aa45b
Description

1 BLISTER PACK in 1 CARTON (67751-221-01) / 8 TABLET, FILM COATED in 1 BLISTER PACK

Marketing

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

Linked Drug Pages (1)

Sominex ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2396151b-13a0-cc41-e063-6394a90aa45b", "openfda": {"unii": ["TC2D6JAD40"], "rxcui": ["1049630", "1086986"], "spl_set_id": ["f70ce1a6-c334-025e-e053-6294a90ae53f"], "manufacturer_name": ["Navajo Manufacturing Company Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (67751-221-01)  / 8 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "67751-221-01", "marketing_start_date": "20120601"}], "brand_name": "Sominex", "product_id": "67751-221_2396151b-13a0-cc41-e063-6394a90aa45b", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "67751-221", "generic_name": "DIPHENHYDRAMINE HYDROCHLORIDE", "labeler_name": "Navajo Manufacturing Company Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Sominex", "active_ingredients": [{"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "M010", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20120601", "listing_expiration_date": "20261231"}