Package 67046-1633-3

Brand: chlorpromazine hydrochloride

Generic: chlorpromazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 67046-1633-3
Digits Only 6704616333
Product NDC 67046-1633
Product ID 67046-1633_472ea988-e54b-93cd-e063-6394a90ada7b
Description

30 TABLET, SUGAR COATED in 1 BLISTER PACK (67046-1633-3)

Marketing

Marketing Status
Marketed Since 2025-12-30
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": "472ea988-e54b-93cd-e063-6394a90ada7b", "openfda": {"unii": ["9WP59609J6"], "rxcui": ["991194"], "spl_set_id": ["472e9a45-4060-3b2a-e063-6294a90a716a"], "manufacturer_name": ["Coupler LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, SUGAR COATED in 1 BLISTER PACK (67046-1633-3)", "package_ndc": "67046-1633-3", "marketing_start_date": "20251230"}], "brand_name": "Chlorpromazine Hydrochloride", "product_id": "67046-1633_472ea988-e54b-93cd-e063-6394a90ada7b", "dosage_form": "TABLET, SUGAR COATED", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "67046-1633", "generic_name": "Chlorpromazine Hydrochloride", "labeler_name": "Coupler LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Chlorpromazine Hydrochloride", "active_ingredients": [{"name": "CHLORPROMAZINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "ANDA214827", "marketing_category": "ANDA", "marketing_start_date": "20251230", "listing_expiration_date": "20261231"}