chlorpromazine hydrochloride
Generic: chlorpromazine hydrochloride
Labeler: novadoz pharmaceuticals llcDrug Facts
Product Profile
Brand Name
chlorpromazine hydrochloride
Generic Name
chlorpromazine hydrochloride
Labeler
novadoz pharmaceuticals llc
Dosage Form
INJECTION
Routes
Active Ingredients
chlorpromazine hydrochloride 25 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
72205-190
Product ID
72205-190_c0c5f94c-5f4d-43db-8cc2-ffc8a45b64cf
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA216092
Listing Expiration
2027-12-31
Marketing Start
2026-01-26
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
72205190
Hyphenated Format
72205-190
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
ANDA216092 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 25 mg/mL
Packaging
- 25 VIAL in 1 CARTON (72205-190-25) / 1 mL in 1 VIAL (72205-190-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR"], "spl_id": "c0c5f94c-5f4d-43db-8cc2-ffc8a45b64cf", "openfda": {"upc": ["0372205190016", "0372205191013"], "unii": ["9WP59609J6"], "rxcui": ["1730076", "1730078"], "spl_set_id": ["c0c5f94c-5f4d-43db-8cc2-ffc8a45b64cf"], "manufacturer_name": ["Novadoz Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 CARTON (72205-190-25) / 1 mL in 1 VIAL (72205-190-01)", "package_ndc": "72205-190-25", "marketing_start_date": "20260202"}], "brand_name": "Chlorpromazine Hydrochloride", "product_id": "72205-190_c0c5f94c-5f4d-43db-8cc2-ffc8a45b64cf", "dosage_form": "INJECTION", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "72205-190", "generic_name": "Chlorpromazine Hydrochloride", "labeler_name": "Novadoz Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Chlorpromazine Hydrochloride", "active_ingredients": [{"name": "CHLORPROMAZINE HYDROCHLORIDE", "strength": "25 mg/mL"}], "application_number": "ANDA216092", "marketing_category": "ANDA", "marketing_start_date": "20260126", "listing_expiration_date": "20271231"}