Package 0404-9942-01

Brand: promethazine hydrochloride

Generic: promethazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0404-9942-01
Digits Only 0404994201
Product NDC 0404-9942
Product ID 0404-9942_b4183b6c-f338-4914-a618-75cb78c0bb7e
Description

1 AMPULE in 1 BAG (0404-9942-01) / 1 mL in 1 AMPULE

Marketing

Marketing Status
Marketed Since 2022-01-17
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": ["INTRAMUSCULAR"], "spl_id": "b4183b6c-f338-4914-a618-75cb78c0bb7e", "openfda": {"unii": ["R61ZEH7I1I"], "rxcui": ["992858"], "spl_set_id": ["c525cb2c-9a01-4a9b-ad2c-08630719953d"], "manufacturer_name": ["Henry Schein, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 AMPULE in 1 BAG (0404-9942-01)  / 1 mL in 1 AMPULE", "package_ndc": "0404-9942-01", "marketing_start_date": "20220117"}], "brand_name": "Promethazine Hydrochloride", "product_id": "0404-9942_b4183b6c-f338-4914-a618-75cb78c0bb7e", "dosage_form": "INJECTION", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "0404-9942", "generic_name": "Promethazine Hydrochloride", "labeler_name": "Henry Schein, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Promethazine Hydrochloride", "active_ingredients": [{"name": "PROMETHAZINE HYDROCHLORIDE", "strength": "50 mg/mL"}], "application_number": "ANDA083312", "marketing_category": "ANDA", "marketing_start_date": "20220117", "listing_expiration_date": "20261231"}