Package 84549-101-25

Brand: diphenhydramine hydrochloride

Generic: diphenhydramine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 84549-101-25
Digits Only 8454910125
Product NDC 84549-101
Description

1 mL in 1 VIAL, SINGLE-DOSE (84549-101-25)

Marketing

Marketing Status
Marketed Since 2025-08-27
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": "463c9f3f-5718-c3fc-e063-6294a90a60aa", "openfda": {"unii": ["TC2D6JAD40"], "rxcui": ["1723740"], "spl_set_id": ["3842d802-9b18-2c5e-e063-6394a90ae763"], "manufacturer_name": ["ProPharma Distribution"]}, "finished": true, "packaging": [{"sample": false, "description": "1 mL in 1 VIAL, SINGLE-DOSE (84549-101-25)", "package_ndc": "84549-101-25", "marketing_start_date": "20250827"}], "brand_name": "Diphenhydramine Hydrochloride", "product_id": "84549-101_463c9f3f-5718-c3fc-e063-6294a90a60aa", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "84549-101", "generic_name": "Diphenhydramine Hydrochloride", "labeler_name": "ProPharma Distribution", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diphenhydramine Hydrochloride", "active_ingredients": [{"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "50 mg/mL"}], "application_number": "ANDA205723", "marketing_category": "ANDA", "marketing_start_date": "20190501", "listing_expiration_date": "20261231"}