Package 25021-481-01

Brand: diphenhydramine hydrochloride

Generic: diphenhydramine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 25021-481-01
Digits Only 2502148101
Product NDC 25021-481
Description

25 VIAL in 1 CARTON (25021-481-01) / 1 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2025-01-15
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": "7521506e-027f-48b1-bd2d-66ad01f01c82", "openfda": {"unii": ["TC2D6JAD40"], "rxcui": ["1723740"], "spl_set_id": ["6533e629-a27b-4489-8fa3-7de32fbf809e"], "manufacturer_name": ["Sagent Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 CARTON (25021-481-01)  / 1 mL in 1 VIAL", "package_ndc": "25021-481-01", "marketing_start_date": "20250115"}], "brand_name": "Diphenhydramine Hydrochloride", "product_id": "25021-481_7521506e-027f-48b1-bd2d-66ad01f01c82", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "25021-481", "generic_name": "Diphenhydramine Hydrochloride", "labeler_name": "Sagent Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diphenhydramine Hydrochloride", "active_ingredients": [{"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "50 mg/mL"}], "application_number": "ANDA218448", "marketing_category": "ANDA", "marketing_start_date": "20250115", "listing_expiration_date": "20261231"}