Package 0904-7131-61

Brand: Chlorpromazine hydrochloride

Generic: Chlorpromazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0904-7131-61
Digits Only 0904713161
Product NDC 0904-7131
Product ID 0904-7131_5f66c7a0-171c-4cc8-8160-99a7b89ea527
Description

100 BLISTER PACK in 1 CARTON (0904-7131-61) / 1 TABLET, FILM COATED in 1 BLISTER PACK

Marketing

Marketing Status
Discontinued 2026-02-28
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": ["ORAL"], "spl_id": "5f66c7a0-171c-4cc8-8160-99a7b89ea527", "openfda": {"unii": ["9WP59609J6"], "rxcui": ["991039", "991044", "991188", "991194", "991336"], "spl_set_id": ["d58570a0-58b0-4662-b2ad-aa8d1463b4c1"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (0904-7131-61)  / 1 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "0904-7131-61", "marketing_end_date": "20260228", "marketing_start_date": "20200127"}], "brand_name": "Chlorpromazine hydrochloride", "product_id": "0904-7131_5f66c7a0-171c-4cc8-8160-99a7b89ea527", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "0904-7131", "generic_name": "Chlorpromazine hydrochloride", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Chlorpromazine hydrochloride", "active_ingredients": [{"name": "CHLORPROMAZINE HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA213368", "marketing_category": "ANDA", "marketing_end_date": "20260228", "marketing_start_date": "20200127"}