Package 60760-456-20

Brand: promethazine hydrochloride

Generic: promethazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 60760-456-20
Digits Only 6076045620
Product NDC 60760-456
Description

20 TABLET in 1 BOTTLE, PLASTIC (60760-456-20)

Marketing

Marketing Status
Marketed Since 2019-10-09
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": "f06eec16-1c20-815e-e053-2995a90afc14", "openfda": {"unii": ["R61ZEH7I1I"], "rxcui": ["992447"], "spl_set_id": ["9492e4e9-cda5-64cc-e053-2995a90a04a5"], "manufacturer_name": ["St. Mary's Medical Park Pharmacy"]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET in 1 BOTTLE, PLASTIC (60760-456-20)", "package_ndc": "60760-456-20", "marketing_start_date": "20191009"}], "brand_name": "Promethazine Hydrochloride", "product_id": "60760-456_f06eec16-1c20-815e-e053-2995a90afc14", "dosage_form": "TABLET", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "60760-456", "generic_name": "Promethazine Hydrochloride", "labeler_name": "St. Mary's Medical Park Pharmacy", "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": "20191009", "listing_expiration_date": "20261231"}