Package 50090-4608-0

Brand: promethazine hydrochloride

Generic: promethazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50090-4608-0
Digits Only 5009046080
Product NDC 50090-4608
Description

90 TABLET in 1 BOTTLE (50090-4608-0)

Marketing

Marketing Status
Marketed Since 2019-10-15
Brand promethazine hydrochloride
Generic promethazine hydrochloride
Sample Package No

Linked Drug Pages (0)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "c3c1637d-7777-4709-8707-aa28fb86db9f", "openfda": {"unii": ["R61ZEH7I1I"], "rxcui": ["992447"], "spl_set_id": ["b54439a3-1d01-4c5f-8508-731790ae215b"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-4608-0)", "package_ndc": "50090-4608-0", "marketing_start_date": "20191015"}], "brand_name": "PROMETHAZINE HYDROCHLORIDE", "product_id": "50090-4608_c3c1637d-7777-4709-8707-aa28fb86db9f", "dosage_form": "TABLET", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "50090-4608", "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": "ANDA040712", "marketing_category": "ANDA", "marketing_start_date": "20060731", "listing_expiration_date": "20261231"}