Package 39822-5550-6

Brand: promethazine hydrochloride

Generic: promethazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 39822-5550-6
Digits Only 3982255506
Product NDC 39822-5550
Description

25 AMPULE in 1 CARTON (39822-5550-6) / 1 mL in 1 AMPULE (39822-5550-5)

Marketing

Marketing Status
Marketed Since 2015-01-30
Brand promethazine hydrochloride
Generic promethazine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "0e860109-725f-1c28-e063-6394a90a50ef", "openfda": {"unii": ["R61ZEH7I1I"], "rxcui": ["992858"], "spl_set_id": ["b6f6698f-f23c-452a-9b38-bbb96ab88ae4"], "manufacturer_name": ["XGen Pharmaceuticals DJB, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 AMPULE in 1 CARTON (39822-5550-6)  / 1 mL in 1 AMPULE (39822-5550-5)", "package_ndc": "39822-5550-6", "marketing_start_date": "20150130"}], "brand_name": "PROMETHAZINE HYDROCHLORIDE", "product_id": "39822-5550_0e860109-725f-1c28-e063-6394a90a50ef", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "39822-5550", "generic_name": "PROMETHAZINE HYDROCHLORIDE", "labeler_name": "XGen Pharmaceuticals DJB, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PROMETHAZINE HYDROCHLORIDE", "active_ingredients": [{"name": "PROMETHAZINE HYDROCHLORIDE", "strength": "50 mg/mL"}], "application_number": "ANDA040737", "marketing_category": "ANDA", "marketing_start_date": "20150130", "listing_expiration_date": "20261231"}