Package 0404-9836-01

Brand: chlorpromazine hydrochloride

Generic: chlorpromazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0404-9836-01
Digits Only 0404983601
Product NDC 0404-9836
Product ID 0404-9836_bf1031fc-2c89-4556-b0df-6d260bf19f94
Description

1 AMPULE in 1 BAG (0404-9836-01) / 1 mL in 1 AMPULE

Marketing

Marketing Status
Marketed Since 2022-01-09
Brand chlorpromazine hydrochloride
Generic chlorpromazine hydrochloride
Sample Package No

Linked Drug Pages (1)

CHLORPROMAZINE HYDROCHLORIDE ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAMUSCULAR"], "spl_id": "bf1031fc-2c89-4556-b0df-6d260bf19f94", "openfda": {"unii": ["9WP59609J6"], "rxcui": ["1730076"], "spl_set_id": ["310d161e-c4db-49e8-8665-d1a6d4e11320"], "manufacturer_name": ["Henry Schein, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 AMPULE in 1 BAG (0404-9836-01)  / 1 mL in 1 AMPULE", "package_ndc": "0404-9836-01", "marketing_start_date": "20220109"}], "brand_name": "CHLORPROMAZINE HYDROCHLORIDE", "product_id": "0404-9836_bf1031fc-2c89-4556-b0df-6d260bf19f94", "dosage_form": "INJECTION", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "0404-9836", "generic_name": "CHLORPROMAZINE HYDROCHLORIDE", "labeler_name": "Henry Schein, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CHLORPROMAZINE HYDROCHLORIDE", "active_ingredients": [{"name": "CHLORPROMAZINE HYDROCHLORIDE", "strength": "25 mg/mL"}], "application_number": "ANDA083329", "marketing_category": "ANDA", "marketing_start_date": "20220109", "listing_expiration_date": "20261231"}