chlorpromazine hydrochloride
Generic: chlorpromazine hydrochloride
Labeler: novadoz pharmaceuticals llcDrug Facts
Product Profile
Brand Name
chlorpromazine hydrochloride
Generic Name
chlorpromazine hydrochloride
Labeler
novadoz pharmaceuticals llc
Dosage Form
TABLET, SUGAR COATED
Routes
Active Ingredients
chlorpromazine hydrochloride 200 mg/1
Manufacturer
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
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
72205107
Hyphenated Format
72205-107
Supplemental Identifiers
RxCUI
UPC
UNII
Packaging Origin
Original Packager
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
source: ndc
Resolved Composition
Strengths
- 200 mg/1
Packaging
- 100 TABLET, SUGAR COATED in 1 BOTTLE (72205-107-91)
Packages (1)
Ingredients (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"}