Package 67046-1563-3

Brand: chlorpromazine hydrochloride

Generic: chlorpromazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 67046-1563-3
Digits Only 6704615633
Product NDC 67046-1563
Product ID 67046-1563_35a7430f-027d-60d9-e063-6294a90a19fc
Description

30 TABLET, SUGAR COATED in 1 BLISTER PACK (67046-1563-3)

Marketing

Marketing Status
Marketed Since 2025-05-21
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": "35a7430f-027d-60d9-e063-6294a90a19fc", "openfda": {"unii": ["9WP59609J6"], "rxcui": ["991336"], "spl_set_id": ["35a743a1-5354-2c50-e063-6394a90a15f9"], "manufacturer_name": ["Coupler LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, SUGAR COATED in 1 BLISTER PACK (67046-1563-3)", "package_ndc": "67046-1563-3", "marketing_start_date": "20250521"}], "brand_name": "Chlorpromazine Hydrochloride", "product_id": "67046-1563_35a7430f-027d-60d9-e063-6294a90a19fc", "dosage_form": "TABLET, SUGAR COATED", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "67046-1563", "generic_name": "Chlorpromazine Hydrochloride", "labeler_name": "Coupler LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Chlorpromazine Hydrochloride", "active_ingredients": [{"name": "CHLORPROMAZINE HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA214827", "marketing_category": "ANDA", "marketing_start_date": "20250521", "listing_expiration_date": "20261231"}