Package 14803-912-00

Brand: Diphenhydramine Hydrochloride 25

Generic: Diphenhydramine Hydrochloride 25
NDC Package

Package Facts

Identity

Package NDC 14803-912-00
Digits Only 1480391200
Product NDC 14803-912
Description

72000 CAPSULE in 1 DRUM (14803-912-00)

Marketing

Marketing Status
Marketed Since 2025-11-01
Brand Diphenhydramine Hydrochloride 25
Generic Diphenhydramine Hydrochloride 25
Sample Package No

Linked Drug Pages (0)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "48ce63d7-e2c5-b448-e063-6294a90a2e94", "openfda": {"unii": ["TC2D6JAD40"], "rxcui": ["1049909"], "spl_set_id": ["3d55914e-0769-2282-e063-6394a90a3a48"], "manufacturer_name": ["Elysium Pharmaceuticals Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "72000 CAPSULE in 1 DRUM (14803-912-00)", "package_ndc": "14803-912-00", "marketing_start_date": "20251101"}], "brand_name": "Diphenhydramine Hydrochloride 25", "product_id": "14803-912_48ce63d7-e2c5-b448-e063-6294a90a2e94", "dosage_form": "CAPSULE", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "14803-912", "generic_name": "Diphenhydramine Hydrochloride 25", "labeler_name": "Elysium Pharmaceuticals Limited", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Diphenhydramine Hydrochloride 25", "active_ingredients": [{"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20250901", "listing_expiration_date": "20271231"}