Package 0363-0714-42

Brand: extra strength nitetime pain relief

Generic: acetaminophen 500 mg,diphenhydramine hydrochloride 25 mg tablet
NDC Package

Package Facts

Identity

Package NDC 0363-0714-42
Digits Only 0363071442
Product NDC 0363-0714
Product ID 0363-0714_3ac05a52-7cce-2bfb-e063-6394a90a134b
Description

1 BOTTLE in 1 CARTON (0363-0714-42) / 24 TABLET in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2021-10-12
Brand extra strength nitetime pain relief
Generic acetaminophen 500 mg,diphenhydramine hydrochloride 25 mg tablet
Sample Package No

Linked Drug Pages (1)

Extra Strength NiteTime Pain Relief ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3ac05a52-7cce-2bfb-e063-6394a90a134b", "openfda": {"unii": ["362O9ITL9D", "TC2D6JAD40"], "rxcui": ["1092189"], "spl_set_id": ["c25c75c7-157f-1c0d-e053-2995a90a2e3c"], "manufacturer_name": ["WALGREENS"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (0363-0714-42)  / 24 TABLET in 1 BOTTLE", "package_ndc": "0363-0714-42", "marketing_start_date": "20211012"}], "brand_name": "Extra Strength NiteTime Pain Relief", "product_id": "0363-0714_3ac05a52-7cce-2bfb-e063-6394a90a134b", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "0363-0714", "generic_name": "Acetaminophen 500 mg,Diphenhydramine Hydrochloride 25 mg Tablet", "labeler_name": "WALGREENS", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Extra Strength NiteTime Pain Relief", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}, {"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20211012", "listing_expiration_date": "20261231"}