chlorpromazine hydrochloride
Generic: chlorpromazine hydrochloride
Labeler: sandoz, inc.Drug Facts
Product Profile
Brand Name
chlorpromazine hydrochloride
Generic Name
chlorpromazine hydrochloride
Labeler
sandoz, inc.
Dosage Form
CONCENTRATE
Routes
Active Ingredients
chlorpromazine hydrochloride 30 mg/mL
Manufacturer
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
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
07814027
Hyphenated Format
0781-4027
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
ANDA214542 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 30 mg/mL
Packaging
- 120 mL in 1 BOTTLE, PLASTIC (0781-4027-53)
Packages (1)
Ingredients (1)
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"}