chlorpromazine

Generic: chlorpromazine

Labeler: alembic pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name chlorpromazine
Generic Name chlorpromazine
Labeler alembic pharmaceuticals inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

chlorpromazine hydrochloride 50 mg/1

Manufacturer
Alembic Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 62332-737
Product ID 62332-737_32f6b72b-6071-43f3-b50b-583e5b557d8e
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA217350
Listing Expiration 2026-12-31
Marketing Start 2023-07-20

Pharmacologic Class

Classes
phenothiazine [epc] phenothiazines [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 62332737
Hyphenated Format 62332-737

Supplemental Identifiers

RxCUI
991039 991044 991188 991194 991336
UPC
0362332739318 0362332736317 0362332738311 0362332737314
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 (source: ndc)
Generic Name chlorpromazine (source: ndc)
Application Number ANDA217350 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 100 BLISTER PACK in 1 CARTON (62332-737-10) / 10 TABLET in 1 BLISTER PACK
  • 100 TABLET in 1 BOTTLE (62332-737-31)
  • 1000 TABLET in 1 BOTTLE (62332-737-91)
source: ndc

Packages (3)

62332-737-10 100 BLISTER PACK in 1 CARTON (62332-737-10) / 10 TABLET in 1 BLISTER PACK 62332-737-31 100 TABLET in 1 BOTTLE (62332-737-31) 62332-737-91 1000 TABLET in 1 BOTTLE (62332-737-91)

Ingredients (1)

chlorpromazine hydrochloride (50 mg/1)

Linked Drug Pages (1)

Chlorpromazine ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "32f6b72b-6071-43f3-b50b-583e5b557d8e", "openfda": {"upc": ["0362332739318", "0362332736317", "0362332738311", "0362332737314"], "unii": ["9WP59609J6"], "rxcui": ["991039", "991044", "991188", "991194", "991336"], "spl_set_id": ["4a0b3268-1d5a-4c98-af77-2461fb488476"], "manufacturer_name": ["Alembic Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (62332-737-10)  / 10 TABLET in 1 BLISTER PACK", "package_ndc": "62332-737-10", "marketing_start_date": "20230720"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (62332-737-31)", "package_ndc": "62332-737-31", "marketing_start_date": "20230720"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (62332-737-91)", "package_ndc": "62332-737-91", "marketing_start_date": "20230720"}], "brand_name": "Chlorpromazine", "product_id": "62332-737_32f6b72b-6071-43f3-b50b-583e5b557d8e", "dosage_form": "TABLET", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "62332-737", "generic_name": "Chlorpromazine", "labeler_name": "Alembic Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Chlorpromazine", "active_ingredients": [{"name": "CHLORPROMAZINE HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA217350", "marketing_category": "ANDA", "marketing_start_date": "20230720", "listing_expiration_date": "20261231"}