chlorpromazine hydrochloride

Generic: chlorpromazine hydrochloride

Labeler: coupler llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name chlorpromazine hydrochloride
Generic Name chlorpromazine hydrochloride
Labeler coupler llc
Dosage Form TABLET, SUGAR COATED
Routes
ORAL
Active Ingredients

chlorpromazine hydrochloride 50 mg/1

Manufacturer
Coupler LLC

Identifiers & Regulatory

Product NDC 67046-1563
Product ID 67046-1563_35a7430f-027d-60d9-e063-6294a90a19fc
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA214827
Listing Expiration 2026-12-31
Marketing Start 2025-05-21

Pharmacologic Class

Classes
phenothiazine [epc] phenothiazines [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 670461563
Hyphenated Format 67046-1563

Supplemental Identifiers

RxCUI
991336
UNII
9WP59609J6

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name chlorpromazine hydrochloride (source: ndc)
Generic Name chlorpromazine hydrochloride (source: ndc)
Application Number ANDA214827 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 30 TABLET, SUGAR COATED in 1 BLISTER PACK (67046-1563-3)
source: ndc

Packages (1)

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

Ingredients (1)

chlorpromazine hydrochloride (50 mg/1)

Linked Drug Pages (1)

Chlorpromazine Hydrochloride ndc-match (0.9)

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"}