Package 80425-0265-1

Brand: promethazine hydrochloride

Generic: promethazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 80425-0265-1
Digits Only 8042502651
Product NDC 80425-0265
Product ID 80425-0265_2a9bad62-b2fe-697c-e063-6294a90aa395
Description

20 TABLET in 1 BOTTLE (80425-0265-1)

Marketing

Marketing Status
Marketed Since 2023-02-15
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": "2a9bad62-b2fe-697c-e063-6294a90aa395", "openfda": {"unii": ["R61ZEH7I1I"], "rxcui": ["992447"], "spl_set_id": ["f4c23037-e415-7604-e053-2995a90a5bb6"], "manufacturer_name": ["Advanced Rx Pharmacy of Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET in 1 BOTTLE (80425-0265-1)", "package_ndc": "80425-0265-1", "marketing_start_date": "20230215"}], "brand_name": "Promethazine Hydrochloride", "product_id": "80425-0265_2a9bad62-b2fe-697c-e063-6294a90aa395", "dosage_form": "TABLET", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "80425-0265", "generic_name": "Promethazine Hydrochloride", "labeler_name": "Advanced Rx Pharmacy of Tennessee, LLC", "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": "20230215", "listing_expiration_date": "20261231"}