Package 71205-521-06

Brand: benadryl

Generic: diphenhydramine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71205-521-06
Digits Only 7120552106
Product NDC 71205-521
Product ID 71205-521_e9c2a959-7772-43f4-a097-535c75b917bd
Description

3 POUCH in 1 BAG (71205-521-06) / 2 TABLET, FILM COATED in 1 POUCH

Marketing

Marketing Status
Marketed Since 2021-01-01
Brand benadryl
Generic diphenhydramine hydrochloride
Sample Package No

Linked Drug Pages (1)

Benadryl ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "e9c2a959-7772-43f4-a097-535c75b917bd", "openfda": {"upc": ["0371205521066"], "unii": ["TC2D6JAD40"], "rxcui": ["1049630", "1049632"], "spl_set_id": ["b1c849e5-8003-4fd3-811d-6a927523e353"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "3 POUCH in 1 BAG (71205-521-06)  / 2 TABLET, FILM COATED in 1 POUCH", "package_ndc": "71205-521-06", "marketing_start_date": "20210101"}], "brand_name": "Benadryl", "product_id": "71205-521_e9c2a959-7772-43f4-a097-535c75b917bd", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "71205-521", "generic_name": "Diphenhydramine Hydrochloride", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Benadryl", "active_ingredients": [{"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20080901", "listing_expiration_date": "20261231"}