Package 51662-1674-1

Brand: diphenhydramine hydrochloride

Generic: diphenhydramine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 51662-1674-1
Digits Only 5166216741
Product NDC 51662-1674
Product ID 51662-1674_44217a8c-7657-a0f6-e063-6294a90af2ad
Description

1 TABLET, FILM COATED in 1 PACKET (51662-1674-1)

Marketing

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

Linked Drug Pages (1)

diphenhydramine hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "44217a8c-7657-a0f6-e063-6294a90af2ad", "openfda": {"unii": ["TC2D6JAD40"], "rxcui": ["1049630"], "spl_set_id": ["44217a8c-7656-a0f6-e063-6294a90af2ad"], "manufacturer_name": ["HF Acquisition Co LLC, DBA HealthFirst"]}, "finished": true, "packaging": [{"sample": false, "description": "1 TABLET, FILM COATED in 1 PACKET (51662-1674-1)", "package_ndc": "51662-1674-1", "marketing_start_date": "20120101"}], "brand_name": "diphenhydramine hydrochloride", "product_id": "51662-1674_44217a8c-7657-a0f6-e063-6294a90af2ad", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "51662-1674", "generic_name": "diphenhydramine hydrochloride", "labeler_name": "HF Acquisition Co LLC, DBA HealthFirst", "product_type": "HUMAN OTC DRUG", "brand_name_base": "diphenhydramine hydrochloride", "active_ingredients": [{"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20120101", "listing_expiration_date": "20261231"}