Package 70518-2488-0

Brand: promethazine hydrochloride

Generic: promethazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-2488-0
Digits Only 7051824880
Product NDC 70518-2488
Product ID 70518-2488_4a2b8d97-b89a-6b68-e063-6394a90ab332
Description

30 TABLET in 1 BLISTER PACK (70518-2488-0)

Marketing

Marketing Status
Marketed Since 2019-12-17
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": "4a2b8d97-b89a-6b68-e063-6394a90ab332", "openfda": {"unii": ["R61ZEH7I1I"], "rxcui": ["992438"], "spl_set_id": ["adb04635-584f-4fef-98ca-2574be312a73"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-2488-0)", "package_ndc": "70518-2488-0", "marketing_start_date": "20191217"}], "brand_name": "Promethazine Hydrochloride", "product_id": "70518-2488_4a2b8d97-b89a-6b68-e063-6394a90ab332", "dosage_form": "TABLET", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "70518-2488", "generic_name": "Promethazine Hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Promethazine Hydrochloride", "active_ingredients": [{"name": "PROMETHAZINE HYDROCHLORIDE", "strength": "12.5 mg/1"}], "application_number": "ANDA040596", "marketing_category": "ANDA", "marketing_start_date": "20191217", "listing_expiration_date": "20271231"}