Package 76168-121-12

Brand: allergy

Generic: diphenhydramine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 76168-121-12
Digits Only 7616812112
Product NDC 76168-121
Description

100 CARTON in 1 BOTTLE (76168-121-12) / 1 TABLET in 1 CARTON

Marketing

Marketing Status
Marketed Since 2018-05-14
Brand allergy
Generic diphenhydramine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "6c30ec6a-4c24-d604-e053-2a91aa0ac869", "openfda": {"unii": ["TC2D6JAD40"], "rxcui": ["1049630"], "spl_set_id": ["73e4f21c-e5ec-42c9-9ec8-118479857057"], "manufacturer_name": ["Velocity Pharma LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CARTON in 1 BOTTLE (76168-121-12)  / 1 TABLET in 1 CARTON", "package_ndc": "76168-121-12", "marketing_start_date": "20180514"}], "brand_name": "Allergy", "product_id": "76168-121_6c30ec6a-4c24-d604-e053-2a91aa0ac869", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "76168-121", "generic_name": "Diphenhydramine Hydrochloride", "labeler_name": "Velocity Pharma LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Allergy", "active_ingredients": [{"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "part341", "marketing_category": "OTC MONOGRAPH FINAL", "marketing_start_date": "20180514", "listing_expiration_date": "20261231"}