chlorpromazine hydrochloride

Generic: chlorpromazine hydrochloride

Labeler: novadoz pharmaceuticals llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

chlorpromazine hydrochloride 200 mg/1

Manufacturer
Novadoz Pharmaceuticals LLC

Identifiers & Regulatory

Product NDC 72205-107
Product ID 72205-107_315ce03f-d9f8-4f3a-9e83-922747430c23
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA214827
Listing Expiration 2026-12-31
Marketing Start 2022-02-09

Pharmacologic Class

Classes
phenothiazine [epc] phenothiazines [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72205107
Hyphenated Format 72205-107

Supplemental Identifiers

RxCUI
991044 991188 991194 991336
UPC
0372205106918 0372205105911 0372205104914 0372205107915
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 ANDA214827 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 200 mg/1
source: ndc
Packaging
  • 100 TABLET, SUGAR COATED in 1 BOTTLE (72205-107-91)
source: ndc

Packages (1)

Ingredients (1)

chlorpromazine hydrochloride (200 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "315ce03f-d9f8-4f3a-9e83-922747430c23", "openfda": {"upc": ["0372205106918", "0372205105911", "0372205104914", "0372205107915"], "unii": ["9WP59609J6"], "rxcui": ["991044", "991188", "991194", "991336"], "spl_set_id": ["315ce03f-d9f8-4f3a-9e83-922747430c23"], "manufacturer_name": ["Novadoz Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, SUGAR COATED in 1 BOTTLE (72205-107-91)", "package_ndc": "72205-107-91", "marketing_start_date": "20220209"}], "brand_name": "Chlorpromazine Hydrochloride", "product_id": "72205-107_315ce03f-d9f8-4f3a-9e83-922747430c23", "dosage_form": "TABLET, SUGAR COATED", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "72205-107", "generic_name": "Chlorpromazine Hydrochloride", "labeler_name": "Novadoz Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Chlorpromazine Hydrochloride", "active_ingredients": [{"name": "CHLORPROMAZINE HYDROCHLORIDE", "strength": "200 mg/1"}], "application_number": "ANDA214827", "marketing_category": "ANDA", "marketing_start_date": "20220209", "listing_expiration_date": "20261231"}