chlorpromazine hydrochloride

Generic: chlorpromazine hydrochloride

Labeler: glenmark pharmaceuticals inc., usa
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name chlorpromazine hydrochloride
Generic Name chlorpromazine hydrochloride
Labeler glenmark pharmaceuticals inc., usa
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

chlorpromazine hydrochloride 200 mg/1

Manufacturer
Glenmark Pharmaceuticals Inc., USA

Identifiers & Regulatory

Product NDC 68462-865
Product ID 68462-865_440a4208-83cc-4ffa-952c-d9c0745c342a
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA212144
Listing Expiration 2026-12-31
Marketing Start 2021-03-23

Pharmacologic Class

Classes
phenothiazine [epc] phenothiazines [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 68462865
Hyphenated Format 68462-865

Supplemental Identifiers

RxCUI
991039 991044 991188 991194 991336
UPC
0368462862018 0368462864012 0368462863015 0368462861011
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 ANDA212144 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 200 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE (68462-865-01)
  • 1000 TABLET, FILM COATED in 1 BOTTLE (68462-865-10)
source: ndc

Packages (2)

68462-865-01 100 TABLET, FILM COATED in 1 BOTTLE (68462-865-01) 68462-865-10 1000 TABLET, FILM COATED in 1 BOTTLE (68462-865-10)

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": "440a4208-83cc-4ffa-952c-d9c0745c342a", "openfda": {"upc": ["0368462862018", "0368462864012", "0368462863015", "0368462861011"], "unii": ["9WP59609J6"], "rxcui": ["991039", "991044", "991188", "991194", "991336"], "spl_set_id": ["a6065ac5-a111-449b-b51b-8bc2907d1ddb"], "manufacturer_name": ["Glenmark Pharmaceuticals Inc., USA"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (68462-865-01)", "package_ndc": "68462-865-01", "marketing_start_date": "20210323"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (68462-865-10)", "package_ndc": "68462-865-10", "marketing_start_date": "20210323"}], "brand_name": "Chlorpromazine Hydrochloride", "product_id": "68462-865_440a4208-83cc-4ffa-952c-d9c0745c342a", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "68462-865", "generic_name": "Chlorpromazine Hydrochloride", "labeler_name": "Glenmark Pharmaceuticals Inc., USA", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Chlorpromazine Hydrochloride", "active_ingredients": [{"name": "CHLORPROMAZINE HYDROCHLORIDE", "strength": "200 mg/1"}], "application_number": "ANDA212144", "marketing_category": "ANDA", "marketing_start_date": "20210323", "listing_expiration_date": "20261231"}