chlorpromazine hci
Generic: chlorpromazine hci
Labeler: dr. reddy's laboratories inc.,Drug Facts
Product Profile
Brand Name
chlorpromazine hci
Generic Name
chlorpromazine hci
Labeler
dr. reddy's laboratories inc.,
Dosage Form
INJECTION
Routes
Active Ingredients
chlorpromazine hydrochloride 25 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
43598-140
Product ID
43598-140_910baac6-1b03-7055-e946-0b4b1b1f043f
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA080365
Listing Expiration
2026-12-31
Marketing Start
2024-09-04
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
43598140
Hyphenated Format
43598-140
Supplemental Identifiers
RxCUI
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 hci (source: ndc)
Generic Name
chlorpromazine hci (source: ndc)
Application Number
ANDA080365 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 25 mg/mL
Packaging
- 25 VIAL in 1 CARTON (43598-140-25) / 1 mL in 1 VIAL (43598-140-11)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR"], "spl_id": "910baac6-1b03-7055-e946-0b4b1b1f043f", "openfda": {"unii": ["9WP59609J6"], "rxcui": ["1730076", "1730078"], "spl_set_id": ["1ec15bce-8a50-9c9a-419a-11b9d58dc5b8"], "manufacturer_name": ["Dr. Reddy's Laboratories Inc.,"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 CARTON (43598-140-25) / 1 mL in 1 VIAL (43598-140-11)", "package_ndc": "43598-140-25", "marketing_start_date": "20240904"}], "brand_name": "CHLORPROMAZINE HCI", "product_id": "43598-140_910baac6-1b03-7055-e946-0b4b1b1f043f", "dosage_form": "INJECTION", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "43598-140", "generic_name": "CHLORPROMAZINE HCI", "labeler_name": "Dr. Reddy's Laboratories Inc.,", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CHLORPROMAZINE HCI", "active_ingredients": [{"name": "CHLORPROMAZINE HYDROCHLORIDE", "strength": "25 mg/mL"}], "application_number": "ANDA080365", "marketing_category": "ANDA", "marketing_start_date": "20240904", "listing_expiration_date": "20261231"}