Package 17714-135-01

Brand: diphenhydramine hydrochloride

Generic: diphenhydramine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 17714-135-01
Digits Only 1771413501
Product NDC 17714-135
Product ID 17714-135_60f4322f-5c99-096a-e053-2a91aa0a64eb
Description

100 TABLET in 1 BOTTLE (17714-135-01)

Marketing

Marketing Status
Marketed Since 2006-09-26
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": "60f4322f-5c99-096a-e053-2a91aa0a64eb", "openfda": {"upc": ["0017714135010"], "unii": ["TC2D6JAD40"], "rxcui": ["1049630"], "spl_set_id": ["c80f9a4c-1055-45d2-8fde-5b57fad3c82a"], "manufacturer_name": ["Advance Pharmaceutical Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (17714-135-01)", "package_ndc": "17714-135-01", "marketing_start_date": "20060926"}], "brand_name": "Diphenhydramine Hydrochloride", "product_id": "17714-135_60f4322f-5c99-096a-e053-2a91aa0a64eb", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "17714-135", "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": "25 mg/1"}], "application_number": "part341", "marketing_category": "OTC MONOGRAPH FINAL", "marketing_start_date": "20060926", "listing_expiration_date": "20261231"}