chlorpromazine hydrochloride

Generic: chlorpromazine hydrochloride

Labeler: aurobindo pharma limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name chlorpromazine hydrochloride
Generic Name chlorpromazine hydrochloride
Labeler aurobindo pharma limited
Dosage Form TABLET
Routes
ORAL
Active Ingredients

chlorpromazine hydrochloride 25 mg/1

Manufacturer
Aurobindo Pharma Limited

Identifiers & Regulatory

Product NDC 59651-568
Product ID 59651-568_eb56a819-e085-4c21-a65e-4b685bde6f3e
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA216788
Listing Expiration 2026-12-31
Marketing Start 2025-04-25

Pharmacologic Class

Classes
phenothiazine [epc] phenothiazines [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 59651568
Hyphenated Format 59651-568

Supplemental Identifiers

RxCUI
991039 991044 991188 991194 991336
UPC
0359651568019
UNII
9WP59609J6

Packaging Origin

Original Packager
true

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 ANDA216788 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (59651-568-01)
  • 1000 TABLET in 1 BOTTLE (59651-568-99)
source: ndc

Packages (2)

59651-568-01 100 TABLET in 1 BOTTLE (59651-568-01) 59651-568-99 1000 TABLET in 1 BOTTLE (59651-568-99)

Ingredients (1)

chlorpromazine hydrochloride (25 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": "eb56a819-e085-4c21-a65e-4b685bde6f3e", "openfda": {"upc": ["0359651568019"], "unii": ["9WP59609J6"], "rxcui": ["991039", "991044", "991188", "991194", "991336"], "spl_set_id": ["c2a8b8a3-187f-4000-bde3-b40bb0e5600f"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (59651-568-01)", "package_ndc": "59651-568-01", "marketing_start_date": "20250425"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (59651-568-99)", "package_ndc": "59651-568-99", "marketing_start_date": "20250425"}], "brand_name": "Chlorpromazine Hydrochloride", "product_id": "59651-568_eb56a819-e085-4c21-a65e-4b685bde6f3e", "dosage_form": "TABLET", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "59651-568", "generic_name": "Chlorpromazine Hydrochloride", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Chlorpromazine Hydrochloride", "active_ingredients": [{"name": "CHLORPROMAZINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "ANDA216788", "marketing_category": "ANDA", "marketing_start_date": "20250425", "listing_expiration_date": "20261231"}