Package 68391-200-79

Brand: berkley and jensen allergy relief

Generic: diphenhydramine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68391-200-79
Digits Only 6839120079
Product NDC 68391-200
Description

400 TABLET in 1 BOTTLE (68391-200-79)

Marketing

Marketing Status
Marketed Since 2013-12-10
Brand berkley and jensen allergy relief
Generic diphenhydramine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "a8ab9724-9b0a-4e3b-b31e-97f0ecb7cceb", "openfda": {"upc": ["0888670018163"], "unii": ["TC2D6JAD40"], "rxcui": ["1049630"], "spl_set_id": ["b52fc311-8853-4116-941b-8be35456abba"], "manufacturer_name": ["BJWC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "400 TABLET in 1 BOTTLE (68391-200-79)", "package_ndc": "68391-200-79", "marketing_start_date": "20131210"}], "brand_name": "Berkley and Jensen Allergy Relief", "product_id": "68391-200_a8ab9724-9b0a-4e3b-b31e-97f0ecb7cceb", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "68391-200", "generic_name": "Diphenhydramine Hydrochloride", "labeler_name": "BJWC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Berkley and Jensen Allergy Relief", "active_ingredients": [{"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20131210", "listing_expiration_date": "20261231"}