Package 90096-131-01

Brand: chlorpromazine hydrochloride

Generic: chlorpromazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 90096-131-01
Digits Only 9009613101
Product NDC 90096-131
Description

100 TABLET, SUGAR COATED in 1 BOTTLE (90096-131-01)

Marketing

Marketing Status
Marketed Since 2022-02-05
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": "2a02dff9-bd37-438d-bac9-ec0fb6faaf09", "openfda": {"unii": ["9WP59609J6"], "rxcui": ["991039", "991044", "991188", "991194", "991336"], "spl_set_id": ["da3c2935-817d-4331-83c3-ed68ba5d35fd"], "manufacturer_name": ["Zameer Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, SUGAR COATED in 1 BOTTLE (90096-131-01)", "package_ndc": "90096-131-01", "marketing_start_date": "20220205"}], "brand_name": "ChlorproMAZINE Hydrochloride", "product_id": "90096-131_2a02dff9-bd37-438d-bac9-ec0fb6faaf09", "dosage_form": "TABLET, SUGAR COATED", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "90096-131", "generic_name": "ChlorproMAZINE Hydrochloride", "labeler_name": "Zameer Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ChlorproMAZINE Hydrochloride", "active_ingredients": [{"name": "CHLORPROMAZINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA212630", "marketing_category": "ANDA", "marketing_start_date": "20220205", "listing_expiration_date": "20261231"}