Package 82706-021-02

Brand: axiv allergy relief

Generic: diphenhydramine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 82706-021-02
Digits Only 8270602102
Product NDC 82706-021
Description

50 POUCH in 1 CARTON (82706-021-02) / 2 TABLET in 1 POUCH

Marketing

Marketing Status
Marketed Since 2024-07-11
Brand axiv 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": "1cd2a6f1-31ae-e507-e063-6394a90aba58", "openfda": {"unii": ["TC2D6JAD40"], "rxcui": ["1049630"], "spl_set_id": ["1cd2a6f1-31ad-e507-e063-6394a90aba58"], "manufacturer_name": ["VIVUNT PHARMA LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "50 POUCH in 1 CARTON (82706-021-02)  / 2 TABLET in 1 POUCH", "package_ndc": "82706-021-02", "marketing_start_date": "20240711"}], "brand_name": "AXIV Allergy Relief", "product_id": "82706-021_1cd2a6f1-31ae-e507-e063-6394a90aba58", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "82706-021", "generic_name": "Diphenhydramine Hydrochloride", "labeler_name": "VIVUNT PHARMA LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "AXIV Allergy Relief", "active_ingredients": [{"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240709", "listing_expiration_date": "20261231"}