Package 42806-649-10

Brand: diphenhydramine hydrochloride

Generic: diphenhydramine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 42806-649-10
Digits Only 4280664910
Product NDC 42806-649
Description

1000 CAPSULE in 1 BOTTLE (42806-649-10)

Marketing

Marketing Status
Marketed Since 2016-11-22
Brand diphenhydramine hydrochloride
Generic diphenhydramine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4884641f-c4af-4148-89c1-0e29c6ec6e5e", "openfda": {"unii": ["TC2D6JAD40"], "rxcui": ["1020477"], "spl_set_id": ["15437a72-24e5-4ef2-b1ea-8d8c0acbcd4c"], "manufacturer_name": ["Epic Pharma, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 CAPSULE in 1 BOTTLE (42806-649-10)", "package_ndc": "42806-649-10", "marketing_start_date": "20161122"}], "brand_name": "Diphenhydramine Hydrochloride", "product_id": "42806-649_4884641f-c4af-4148-89c1-0e29c6ec6e5e", "dosage_form": "CAPSULE", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "42806-649", "generic_name": "Diphenhydramine Hydrochloride", "labeler_name": "Epic Pharma, LLC", "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": "20161122", "listing_expiration_date": "20261231"}