Package 70264-024-01

Brand: benadryl allergy

Generic: diphenhydramine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70264-024-01
Digits Only 7026402401
Product NDC 70264-024
Product ID 70264-024_43c8a290-73a2-52bb-e063-6294a90af527
Description

30 POUCH in 1 CARTON (70264-024-01) / 2 TABLET, FILM COATED in 1 POUCH

Marketing

Marketing Status
Marketed Since 2022-12-26
Brand benadryl allergy
Generic diphenhydramine hydrochloride
Sample Package No

Linked Drug Pages (1)

Benadryl Allergy ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "43c8a290-73a2-52bb-e063-6294a90af527", "openfda": {"unii": ["TC2D6JAD40"], "rxcui": ["1049630", "1049632"], "spl_set_id": ["c46c01c0-29f4-400c-bef5-14b3eb944c51"], "manufacturer_name": ["R J General Corporation"]}, "finished": true, "packaging": [{"sample": false, "description": "30 POUCH in 1 CARTON (70264-024-01)  / 2 TABLET, FILM COATED in 1 POUCH", "package_ndc": "70264-024-01", "marketing_start_date": "20221226"}], "brand_name": "Benadryl Allergy", "product_id": "70264-024_43c8a290-73a2-52bb-e063-6294a90af527", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "70264-024", "generic_name": "DIPHENHYDRAMINE HYDROCHLORIDE", "labeler_name": "R J General Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Benadryl Allergy", "active_ingredients": [{"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20220301", "listing_expiration_date": "20261231"}