Package 73629-001-22

Brand: diphenhydramine hydrochloride 50mg

Generic: diphenhydramine hydrochloride 50mg
NDC Package

Package Facts

Identity

Package NDC 73629-001-22
Digits Only 7362900122
Product NDC 73629-001
Description

220 CAPSULE, LIQUID FILLED in 1 BOTTLE (73629-001-22)

Marketing

Marketing Status
Marketed Since 2020-09-28
Brand diphenhydramine hydrochloride 50mg
Generic diphenhydramine hydrochloride 50mg
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "47d40d86-cbe8-fc70-e063-6394a90a2ff3", "openfda": {"unii": ["TC2D6JAD40"], "rxcui": ["1020477"], "spl_set_id": ["af0b1b08-e269-6399-e053-2a95a90ac12d"], "manufacturer_name": ["AMZ789 LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "220 CAPSULE, LIQUID FILLED in 1 BOTTLE (73629-001-22)", "package_ndc": "73629-001-22", "marketing_start_date": "20200928"}], "brand_name": "DIPHENHYDRAMINE HYDROCHLORIDE 50mg", "product_id": "73629-001_47d40d86-cbe8-fc70-e063-6394a90a2ff3", "dosage_form": "CAPSULE, LIQUID FILLED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "73629-001", "generic_name": "DIPHENHYDRAMINE HYDROCHLORIDE 50mg", "labeler_name": "AMZ789 LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "DIPHENHYDRAMINE HYDROCHLORIDE 50mg", "active_ingredients": [{"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "M010", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20200921", "listing_expiration_date": "20271231"}