chlorpromazine hydrochloride

Generic: chlorpromazine

Labeler: sun pharmaceutical industries inc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name chlorpromazine hydrochloride
Generic Name chlorpromazine
Labeler sun pharmaceutical industries inc
Dosage Form TABLET, SUGAR COATED
Routes
ORAL
Active Ingredients

chlorpromazine hydrochloride 200 mg/1

Manufacturer
Sun Pharmaceutical Industries Inc

Identifiers & Regulatory

Product NDC 63304-083
Product ID 63304-083_c2d3824b-8e6f-414d-aa16-de9e2d448645
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA214256
Listing Expiration 2026-12-31
Marketing Start 2020-11-18

Pharmacologic Class

Classes
phenothiazine [epc] phenothiazines [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 63304083
Hyphenated Format 63304-083

Supplemental Identifiers

RxCUI
991039 991044 991188 991194 991336
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 (source: ndc)
Application Number ANDA214256 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 200 mg/1
source: ndc
Packaging
  • 100 TABLET, SUGAR COATED in 1 BOTTLE (63304-083-01)
  • 1000 TABLET, SUGAR COATED in 1 BOTTLE (63304-083-10)
source: ndc

Packages (2)

63304-083-01 100 TABLET, SUGAR COATED in 1 BOTTLE (63304-083-01) 63304-083-10 1000 TABLET, SUGAR COATED in 1 BOTTLE (63304-083-10)

Ingredients (1)

chlorpromazine hydrochloride (200 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": "c2d3824b-8e6f-414d-aa16-de9e2d448645", "openfda": {"unii": ["9WP59609J6"], "rxcui": ["991039", "991044", "991188", "991194", "991336"], "spl_set_id": ["432cd4ca-c728-48ff-beec-2485f5e02512"], "manufacturer_name": ["Sun Pharmaceutical Industries Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, SUGAR COATED in 1 BOTTLE (63304-083-01)", "package_ndc": "63304-083-01", "marketing_start_date": "20201118"}, {"sample": false, "description": "1000 TABLET, SUGAR COATED in 1 BOTTLE (63304-083-10)", "package_ndc": "63304-083-10", "marketing_start_date": "20201118"}], "brand_name": "ChlorproMAZINE Hydrochloride", "product_id": "63304-083_c2d3824b-8e6f-414d-aa16-de9e2d448645", "dosage_form": "TABLET, SUGAR COATED", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "63304-083", "generic_name": "ChlorproMAZINE", "labeler_name": "Sun Pharmaceutical Industries Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ChlorproMAZINE Hydrochloride", "active_ingredients": [{"name": "CHLORPROMAZINE HYDROCHLORIDE", "strength": "200 mg/1"}], "application_number": "ANDA214256", "marketing_category": "ANDA", "marketing_start_date": "20201118", "listing_expiration_date": "20261231"}