chlorpromazine hydrochloride

Generic: chlorpromazine hydrochloride

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

Drug Facts

Product Profile

Brand Name chlorpromazine hydrochloride
Generic Name chlorpromazine hydrochloride
Labeler amneal pharmaceuticals ny llc
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

chlorpromazine hydrochloride 25 mg/1

Manufacturer
Amneal Pharmaceuticals NY LLC

Identifiers & Regulatory

Product NDC 69238-1056
Product ID 69238-1056_9e50c657-1fae-40c2-af7e-e3c389dd5a6d
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA209755
Listing Expiration 2027-12-31
Marketing Start 2018-09-12

Pharmacologic Class

Classes
phenothiazine [epc] phenothiazines [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 692381056
Hyphenated Format 69238-1056

Supplemental Identifiers

RxCUI
991039 991044 991188 991194 991336
UPC
0369238105612 0369238106213
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 ANDA209755 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE (69238-1056-1)
source: ndc

Packages (1)

69238-1056-1 100 TABLET, FILM COATED in 1 BOTTLE (69238-1056-1)

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": "9e50c657-1fae-40c2-af7e-e3c389dd5a6d", "openfda": {"upc": ["0369238105612", "0369238106213"], "unii": ["9WP59609J6"], "rxcui": ["991039", "991044", "991188", "991194", "991336"], "spl_set_id": ["aa086a21-de85-4b03-af58-49b70acf8cf0"], "manufacturer_name": ["Amneal Pharmaceuticals NY LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (69238-1056-1)", "package_ndc": "69238-1056-1", "marketing_start_date": "20180912"}], "brand_name": "CHLORPROMAZINE HYDROCHLORIDE", "product_id": "69238-1056_9e50c657-1fae-40c2-af7e-e3c389dd5a6d", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "69238-1056", "generic_name": "CHLORPROMAZINE HYDROCHLORIDE", "labeler_name": "Amneal Pharmaceuticals NY LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CHLORPROMAZINE HYDROCHLORIDE", "active_ingredients": [{"name": "CHLORPROMAZINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "ANDA209755", "marketing_category": "ANDA", "marketing_start_date": "20180912", "listing_expiration_date": "20271231"}