chlorpromazine hydrochloride

Generic: chlorpromazine hydrochloride

Labeler: sandoz, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name chlorpromazine hydrochloride
Generic Name chlorpromazine hydrochloride
Labeler sandoz, inc.
Dosage Form CONCENTRATE
Routes
ORAL
Active Ingredients

chlorpromazine hydrochloride 30 mg/mL

Manufacturer
Sandoz, Inc.

Identifiers & Regulatory

Product NDC 0781-4027
Product ID 0781-4027_cfff95df-4926-4139-a109-2beebebcf014
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA214542
Listing Expiration 2026-12-31
Marketing Start 2023-03-31

Pharmacologic Class

Classes
phenothiazine [epc] phenothiazines [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 07814027
Hyphenated Format 0781-4027

Supplemental Identifiers

RxCUI
991053 991332
UPC
0307814028221 0307814027538
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 ANDA214542 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 30 mg/mL
source: ndc
Packaging
  • 120 mL in 1 BOTTLE, PLASTIC (0781-4027-53)
source: ndc

Packages (1)

Ingredients (1)

chlorpromazine hydrochloride (30 mg/mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "cfff95df-4926-4139-a109-2beebebcf014", "openfda": {"upc": ["0307814028221", "0307814027538"], "unii": ["9WP59609J6"], "rxcui": ["991053", "991332"], "spl_set_id": ["9398a0b4-e08b-4eb7-9f31-97d4f384427a"], "manufacturer_name": ["Sandoz, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "120 mL in 1 BOTTLE, PLASTIC (0781-4027-53)", "package_ndc": "0781-4027-53", "marketing_start_date": "20230331"}], "brand_name": "Chlorpromazine Hydrochloride", "product_id": "0781-4027_cfff95df-4926-4139-a109-2beebebcf014", "dosage_form": "CONCENTRATE", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "0781-4027", "generic_name": "Chlorpromazine Hydrochloride", "labeler_name": "Sandoz, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Chlorpromazine Hydrochloride", "active_ingredients": [{"name": "CHLORPROMAZINE HYDROCHLORIDE", "strength": "30 mg/mL"}], "application_number": "ANDA214542", "marketing_category": "ANDA", "marketing_start_date": "20230331", "listing_expiration_date": "20261231"}