Package 37835-641-01

Brand: diphenhydramine hydrochloride

Generic: diphenhydramine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 37835-641-01
Digits Only 3783564101
Product NDC 37835-641
Description

100 TABLET in 1 BOTTLE (37835-641-01)

Marketing

Marketing Status
Marketed Since 2025-02-01
Brand diphenhydramine hydrochloride
Generic diphenhydramine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "38f71fd9-448b-95d3-e063-6294a90a3523", "openfda": {"upc": ["0071357006915"], "unii": ["TC2D6JAD40"], "rxcui": ["1049630"], "spl_set_id": ["2e7a9032-67d6-d408-e063-6394a90aca8c"], "manufacturer_name": ["Bi-Mart"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (37835-641-01)", "package_ndc": "37835-641-01", "marketing_start_date": "20250201"}], "brand_name": "Diphenhydramine Hydrochloride", "product_id": "37835-641_38f71fd9-448b-95d3-e063-6294a90a3523", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "37835-641", "generic_name": "Diphenhydramine Hydrochloride", "labeler_name": "Bi-Mart", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Diphenhydramine Hydrochloride", "active_ingredients": [{"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20250201", "listing_expiration_date": "20261231"}