chlorpromazine hydrochloride

Generic: chlorpromazine hydrochloride

Labeler: chartwell rx, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

chlorpromazine hydrochloride 100 mg/1

Manufacturer
Chartwell RX, LLC

Identifiers & Regulatory

Product NDC 62135-423
Product ID 62135-423_459bb2f6-3a40-6998-e063-6394a90a7e2f
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA212630
Listing Expiration 2026-12-31
Marketing Start 2022-02-05

Pharmacologic Class

Classes
phenothiazine [epc] phenothiazines [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 62135423
Hyphenated Format 62135-423

Supplemental Identifiers

RxCUI
991039 991044 991188 991194 991336
UPC
0362135420901 0362135422905 0362135424909 0362135421908 0362135423902
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 ANDA212630 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 90 TABLET, SUGAR COATED in 1 BOTTLE (62135-423-90)
source: ndc

Packages (1)

62135-423-90 90 TABLET, SUGAR COATED in 1 BOTTLE (62135-423-90)

Ingredients (1)

chlorpromazine hydrochloride (100 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": "459bb2f6-3a40-6998-e063-6394a90a7e2f", "openfda": {"upc": ["0362135420901", "0362135422905", "0362135424909", "0362135421908", "0362135423902"], "unii": ["9WP59609J6"], "rxcui": ["991039", "991044", "991188", "991194", "991336"], "spl_set_id": ["e9d6a9e9-ba25-4c25-9b03-25897a3ac5f3"], "manufacturer_name": ["Chartwell RX, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, SUGAR COATED in 1 BOTTLE (62135-423-90)", "package_ndc": "62135-423-90", "marketing_start_date": "20221020"}], "brand_name": "chlorpromazine hydrochloride", "product_id": "62135-423_459bb2f6-3a40-6998-e063-6394a90a7e2f", "dosage_form": "TABLET, SUGAR COATED", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "62135-423", "generic_name": "chlorpromazine hydrochloride", "labeler_name": "Chartwell RX, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "chlorpromazine hydrochloride", "active_ingredients": [{"name": "CHLORPROMAZINE HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA212630", "marketing_category": "ANDA", "marketing_start_date": "20220205", "listing_expiration_date": "20261231"}