Package 51662-1348-1

Brand: diphenhydramine hydrochloride

Generic: diphenhydramine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 51662-1348-1
Digits Only 5166213481
Product NDC 51662-1348
Product ID 51662-1348_ef7bd6e6-d62c-7e93-e053-2a95a90aef83
Description

1 mL in 1 VIAL (51662-1348-1)

Marketing

Marketing Status
Marketed Since 2018-11-26
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": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "ef7bd6e6-d62c-7e93-e053-2a95a90aef83", "openfda": {"unii": ["TC2D6JAD40"], "rxcui": ["1723740"], "spl_set_id": ["7b9ed8ef-ce21-19e7-e053-2a91aa0a81be"], "manufacturer_name": ["HF Acquisition Co LLC, DBA HealthFirst"]}, "finished": true, "packaging": [{"sample": false, "description": "1 mL in 1 VIAL (51662-1348-1)", "package_ndc": "51662-1348-1", "marketing_start_date": "20181126"}], "brand_name": "DIPHENHYDRAMINE HYDROCHLORIDE", "product_id": "51662-1348_ef7bd6e6-d62c-7e93-e053-2a95a90aef83", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "51662-1348", "generic_name": "DIPHENHYDRAMINE HYDROCHLORIDE", "labeler_name": "HF Acquisition Co LLC, DBA HealthFirst", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DIPHENHYDRAMINE HYDROCHLORIDE", "active_ingredients": [{"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "50 mg/mL"}], "application_number": "ANDA040466", "marketing_category": "ANDA", "marketing_start_date": "20181126", "listing_expiration_date": "20261231"}