Package 70518-4419-0

Brand: promethazine hydrochloride

Generic: promethazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-4419-0
Digits Only 7051844190
Product NDC 70518-4419
Product ID 70518-4419_40409092-2986-8b75-e063-6394a90af407
Description

30 TABLET in 1 BLISTER PACK (70518-4419-0)

Marketing

Marketing Status
Marketed Since 2025-07-31
Brand promethazine hydrochloride
Generic promethazine hydrochloride
Sample Package No

Linked Drug Pages (1)

Promethazine Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "40409092-2986-8b75-e063-6394a90af407", "openfda": {"unii": ["R61ZEH7I1I"], "rxcui": ["992447"], "spl_set_id": ["6728bb41-5d50-4abb-bb73-993dcc16ee66"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-4419-0)", "package_ndc": "70518-4419-0", "marketing_start_date": "20250731"}], "brand_name": "Promethazine Hydrochloride", "product_id": "70518-4419_40409092-2986-8b75-e063-6394a90af407", "dosage_form": "TABLET", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "70518-4419", "generic_name": "Promethazine Hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Promethazine Hydrochloride", "active_ingredients": [{"name": "PROMETHAZINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "ANDA040596", "marketing_category": "ANDA", "marketing_start_date": "20250731", "listing_expiration_date": "20261231"}