Package 53209-3001-2

Brand: benadryl

Generic: diphenhydramine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 53209-3001-2
Digits Only 5320930012
Product NDC 53209-3001
Product ID 53209-3001_371fa3fe-9460-112b-e063-6294a90afe82
Description

25 BLISTER PACK in 1 PACKET (53209-3001-2) / 2 TABLET, FILM COATED in 1 BLISTER PACK (53209-3001-1)

Marketing

Marketing Status
Marketed Since 2025-06-09
Brand benadryl
Generic diphenhydramine hydrochloride
Sample Package No

Linked Drug Pages (1)

Benadryl ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "371fa3fe-9460-112b-e063-6294a90afe82", "openfda": {"unii": ["TC2D6JAD40"], "rxcui": ["1049630", "1049632"], "spl_set_id": ["f4ff84b3-bb0c-4900-8ba4-6d1b90394782"], "manufacturer_name": ["Morning Star OTC"]}, "finished": true, "packaging": [{"sample": false, "description": "25 BLISTER PACK in 1 PACKET (53209-3001-2)  / 2 TABLET, FILM COATED in 1 BLISTER PACK (53209-3001-1)", "package_ndc": "53209-3001-2", "marketing_start_date": "20250609"}], "brand_name": "Benadryl", "product_id": "53209-3001_371fa3fe-9460-112b-e063-6294a90afe82", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "53209-3001", "generic_name": "Diphenhydramine Hydrochloride", "labeler_name": "Morning Star OTC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Benadryl", "active_ingredients": [{"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20250609", "listing_expiration_date": "20261231"}