Package 50332-0150-4

Brand: histaprin

Generic: diphenhydramine
NDC Package

Package Facts

Identity

Package NDC 50332-0150-4
Digits Only 5033201504
Product NDC 50332-0150
Description

50 PACKET in 1 BOX, UNIT-DOSE (50332-0150-4) / 1 TABLET in 1 PACKET

Marketing

Marketing Status
Marketed Since 2023-01-01
Brand histaprin
Generic diphenhydramine
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "675ce74c-0894-4272-85ba-086f33459a9a", "openfda": {"unii": ["TC2D6JAD40"], "rxcui": ["1049630"], "spl_set_id": ["38786a65-a12b-4479-b63c-b7c15410da04"], "manufacturer_name": ["NorMed"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "50 PACKET in 1 BOX, UNIT-DOSE (50332-0150-4)  / 1 TABLET in 1 PACKET", "package_ndc": "50332-0150-4", "marketing_start_date": "20230101"}], "brand_name": "HISTAPRIN", "product_id": "50332-0150_675ce74c-0894-4272-85ba-086f33459a9a", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "50332-0150", "generic_name": "Diphenhydramine", "labeler_name": "NorMed", "product_type": "HUMAN OTC DRUG", "brand_name_base": "HISTAPRIN", "active_ingredients": [{"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "M", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20230101", "listing_expiration_date": "20271231"}