Package 57631-010-00

Brand: acetaminophen and diphenhydramine citrate

Generic: acetaminophen and diphenhydramine citrate
NDC Package

Package Facts

Identity

Package NDC 57631-010-00
Digits Only 5763101000
Product NDC 57631-010
Description

30000 TABLET in 1 BOX (57631-010-00)

Marketing

Marketing Status
Marketed Since 2025-10-01
Brand acetaminophen and diphenhydramine citrate
Generic acetaminophen and diphenhydramine citrate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "403a87a6-fe92-8e79-e063-6394a90a70ce", "openfda": {"unii": ["362O9ITL9D", "4OD433S209"], "rxcui": ["1099872"], "spl_set_id": ["403a88fa-e06b-9b6e-e063-6394a90a97b8"], "manufacturer_name": ["InvaTech Pharma Solutions LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30000 TABLET in 1 BOX (57631-010-00)", "package_ndc": "57631-010-00", "marketing_start_date": "20251001"}], "brand_name": "Acetaminophen and Diphenhydramine citrate", "product_id": "57631-010_403a87a6-fe92-8e79-e063-6394a90a70ce", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "57631-010", "generic_name": "Acetaminophen and Diphenhydramine citrate", "labeler_name": "InvaTech Pharma Solutions LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Acetaminophen and Diphenhydramine citrate", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}, {"name": "DIPHENHYDRAMINE CITRATE", "strength": "38 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20251001", "listing_expiration_date": "20261231"}