Package 50090-4812-0

Brand: promethazine hydrochloride

Generic: promethazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50090-4812-0
Digits Only 5009048120
Product NDC 50090-4812
Description

90 TABLET in 1 BOTTLE (50090-4812-0)

Marketing

Marketing Status
Marketed Since 2019-12-27
Brand promethazine hydrochloride
Generic promethazine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "539f36e4-e67b-4d3f-98a4-cf307f22e42a", "openfda": {"unii": ["R61ZEH7I1I"], "rxcui": ["992447"], "spl_set_id": ["87429921-00d2-42c7-9e99-600e8075b8ce"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-4812-0)", "package_ndc": "50090-4812-0", "marketing_start_date": "20191227"}], "brand_name": "Promethazine Hydrochloride", "product_id": "50090-4812_539f36e4-e67b-4d3f-98a4-cf307f22e42a", "dosage_form": "TABLET", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "50090-4812", "generic_name": "Promethazine Hydrochloride", "labeler_name": "A-S Medication Solutions", "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": "20051214", "listing_expiration_date": "20261231"}