Package 55681-323-03

Brand: allergy relief

Generic: diphenhydramine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 55681-323-03
Digits Only 5568132303
Product NDC 55681-323
Product ID 55681-323_3906f36f-58a1-4299-e063-6394a90a30df
Description

300 TABLET in 1 BOTTLE (55681-323-03)

Marketing

Marketing Status
Marketed Since 2024-11-01
Brand allergy relief
Generic diphenhydramine hydrochloride
Sample Package No

Linked Drug Pages (1)

Allergy Relief ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3906f36f-58a1-4299-e063-6394a90a30df", "openfda": {"unii": ["TC2D6JAD40"], "rxcui": ["1049630"], "spl_set_id": ["7b000478-649d-4511-b3e0-eea6995b9784"], "manufacturer_name": ["TWIN MED LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "300 TABLET in 1 BOTTLE (55681-323-03)", "package_ndc": "55681-323-03", "marketing_start_date": "20241101"}], "brand_name": "Allergy Relief", "product_id": "55681-323_3906f36f-58a1-4299-e063-6394a90a30df", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "55681-323", "generic_name": "Diphenhydramine Hydrochloride", "labeler_name": "TWIN MED LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Allergy Relief", "active_ingredients": [{"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20241101", "listing_expiration_date": "20261231"}