chlorpromazine hydrochloride
Generic: chlorpromazine hydrochloride
Labeler: camber pharmaceuticals, inc.Drug Facts
Product Profile
Brand Name
chlorpromazine hydrochloride
Generic Name
chlorpromazine hydrochloride
Labeler
camber pharmaceuticals, inc.
Dosage Form
INJECTION
Routes
Active Ingredients
chlorpromazine hydrochloride 25 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
31722-366
Product ID
31722-366_2d38c8d4-8ed5-0840-e063-6294a90a904f
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA218272
Listing Expiration
2026-12-31
Marketing Start
2024-11-18
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
31722366
Hyphenated Format
31722-366
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
ANDA218272 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 25 mg/mL
Packaging
- 25 VIAL in 1 CARTON (31722-366-32) / 1 mL in 1 VIAL (31722-366-31)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR"], "spl_id": "2d38c8d4-8ed5-0840-e063-6294a90a904f", "openfda": {"upc": ["0331722367318"], "unii": ["9WP59609J6"], "rxcui": ["1730076", "1730078"], "spl_set_id": ["6564346c-661c-41cf-9cef-db6aa15710cd"], "manufacturer_name": ["Camber Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 CARTON (31722-366-32) / 1 mL in 1 VIAL (31722-366-31)", "package_ndc": "31722-366-32", "marketing_start_date": "20241118"}], "brand_name": "CHLORPROMAZINE HYDROCHLORIDE", "product_id": "31722-366_2d38c8d4-8ed5-0840-e063-6294a90a904f", "dosage_form": "INJECTION", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "31722-366", "generic_name": "chlorpromazine hydrochloride", "labeler_name": "Camber Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CHLORPROMAZINE HYDROCHLORIDE", "active_ingredients": [{"name": "CHLORPROMAZINE HYDROCHLORIDE", "strength": "25 mg/mL"}], "application_number": "ANDA218272", "marketing_category": "ANDA", "marketing_start_date": "20241118", "listing_expiration_date": "20261231"}