Package 17714-023-50

Brand: diphenhydramine hydrochloride

Generic: diphenhydramine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 17714-023-50
Digits Only 1771402350
Product NDC 17714-023
Product ID 17714-023_5cc9196c-68d7-c9c1-e053-2a91aa0acd8b
Description

50 TABLET in 1 BOTTLE (17714-023-50)

Marketing

Marketing Status
Marketed Since 2012-09-01
Brand diphenhydramine hydrochloride
Generic diphenhydramine hydrochloride
Sample Package No

Linked Drug Pages (1)

Diphenhydramine Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "5cc9196c-68d7-c9c1-e053-2a91aa0acd8b", "openfda": {"unii": ["TC2D6JAD40"], "rxcui": ["1085945"], "spl_set_id": ["d1f51b7b-da65-4637-8199-f7d59e6dd1c1"], "manufacturer_name": ["Advance Pharmaceutical Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "50 TABLET in 1 BOTTLE (17714-023-50)", "package_ndc": "17714-023-50", "marketing_start_date": "20120901"}], "brand_name": "Diphenhydramine Hydrochloride", "product_id": "17714-023_5cc9196c-68d7-c9c1-e053-2a91aa0acd8b", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "17714-023", "generic_name": "Diphenhydramine Hydrochloride", "labeler_name": "Advance Pharmaceutical Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Diphenhydramine Hydrochloride", "active_ingredients": [{"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "part341", "marketing_category": "OTC MONOGRAPH FINAL", "marketing_start_date": "20120901", "listing_expiration_date": "20261231"}