Package 0404-9851-01

Brand: diphenhydramine hydrochloride

Generic: diphenhydramine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0404-9851-01
Digits Only 0404985101
Product NDC 0404-9851
Description

1 VIAL, SINGLE-DOSE in 1 BAG (0404-9851-01) / 1 mL in 1 VIAL, SINGLE-DOSE

Marketing

Marketing Status
Marketed Since 2022-01-17
Brand diphenhydramine hydrochloride
Generic diphenhydramine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "6bcc631f-5945-4ce5-912d-9fb3403e3670", "openfda": {"unii": ["TC2D6JAD40"], "rxcui": ["1723740"], "spl_set_id": ["af972e71-62ab-40c6-925a-cbcb4d6720a4"], "manufacturer_name": ["Henry Schein, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 BAG (0404-9851-01)  / 1 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "0404-9851-01", "marketing_start_date": "20220117"}], "brand_name": "Diphenhydramine Hydrochloride", "product_id": "0404-9851_6bcc631f-5945-4ce5-912d-9fb3403e3670", "dosage_form": "INJECTION", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "0404-9851", "generic_name": "Diphenhydramine Hydrochloride", "labeler_name": "Henry Schein, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diphenhydramine Hydrochloride", "active_ingredients": [{"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "50 mg/mL"}], "application_number": "ANDA080817", "marketing_category": "ANDA", "marketing_start_date": "20220117", "listing_expiration_date": "20261231"}