Package 51407-436-01

Brand: chlorpromazine hydrochloride

Generic: chlorpromazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 51407-436-01
Digits Only 5140743601
Product NDC 51407-436
Description

100 TABLET, COATED in 1 BOTTLE (51407-436-01)

Marketing

Marketing Status
Marketed Since 2021-02-16
Brand chlorpromazine hydrochloride
Generic chlorpromazine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "45b74177-0987-aecc-e063-6294a90a1625", "openfda": {"unii": ["9WP59609J6"], "rxcui": ["991039", "991044", "991188", "991194", "991336"], "spl_set_id": ["c212a2a1-323a-8b61-e053-2995a90a5b04"], "manufacturer_name": ["Golden State Medical Supply, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, COATED in 1 BOTTLE (51407-436-01)", "package_ndc": "51407-436-01", "marketing_start_date": "20210216"}], "brand_name": "Chlorpromazine Hydrochloride", "product_id": "51407-436_45b74177-0987-aecc-e063-6294a90a1625", "dosage_form": "TABLET, COATED", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "51407-436", "generic_name": "Chlorpromazine Hydrochloride", "labeler_name": "Golden State Medical Supply, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Chlorpromazine Hydrochloride", "active_ingredients": [{"name": "CHLORPROMAZINE HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA212996", "marketing_category": "ANDA", "marketing_start_date": "20210122", "listing_expiration_date": "20261231"}