Package 69721-005-30

Brand: somnapure clinical strength

Generic: diphenhydramine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 69721-005-30
Digits Only 6972100530
Product NDC 69721-005
Product ID 69721-005_35de71a0-7e1c-45fb-97d1-ddf485df6e3c
Description

1 BOTTLE in 1 CARTON (69721-005-30) / 30 TABLET, COATED in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2018-03-20
Brand somnapure clinical strength
Generic diphenhydramine hydrochloride
Sample Package No

Linked Drug Pages (1)

Somnapure Clinical Strength ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "35de71a0-7e1c-45fb-97d1-ddf485df6e3c", "openfda": {"unii": ["TC2D6JAD40"], "rxcui": ["1085945", "1609070"], "spl_set_id": ["063517c0-bcb1-46dd-85f1-bbb2f24274ef"], "manufacturer_name": ["Force Factor Brands LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (69721-005-30)  / 30 TABLET, COATED in 1 BOTTLE", "package_ndc": "69721-005-30", "marketing_start_date": "20180320"}], "brand_name": "Somnapure Clinical Strength", "product_id": "69721-005_35de71a0-7e1c-45fb-97d1-ddf485df6e3c", "dosage_form": "TABLET, COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "69721-005", "generic_name": "Diphenhydramine Hydrochloride", "labeler_name": "Force Factor Brands LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Somnapure", "brand_name_suffix": "Clinical Strength", "active_ingredients": [{"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "M010", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20180320", "listing_expiration_date": "20261231"}