chlorpromazine hydrochloride

Generic: chlorpromazine hydrochloride

Labeler: fresenius kabi usa, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name chlorpromazine hydrochloride
Generic Name chlorpromazine hydrochloride
Labeler fresenius kabi usa, llc
Dosage Form INJECTION
Routes
INTRAMUSCULAR
Active Ingredients

chlorpromazine hydrochloride 25 mg/mL

Manufacturer
Fresenius Kabi USA, LLC

Identifiers & Regulatory

Product NDC 65219-130
Product ID 65219-130_64ba1614-82e8-476f-957d-a29198c7a26e
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA216724
Listing Expiration 2026-12-31
Marketing Start 2025-02-15

Pharmacologic Class

Classes
phenothiazine [epc] phenothiazines [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 65219130
Hyphenated Format 65219-130

Supplemental Identifiers

RxCUI
1730076 1730078
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 ANDA216724 (source: ndc)
Routes
INTRAMUSCULAR
source: ndc

Resolved Composition

Strengths
  • 25 mg/mL
source: ndc
Packaging
  • 25 VIAL in 1 CARTON (65219-130-02) / 2 mL in 1 VIAL (65219-130-01)
source: ndc

Packages (1)

65219-130-02 25 VIAL in 1 CARTON (65219-130-02) / 2 mL in 1 VIAL (65219-130-01)

Ingredients (1)

chlorpromazine hydrochloride (25 mg/mL)

Linked Drug Pages (1)

CHLORPROMAZINE HYDROCHLORIDE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAMUSCULAR"], "spl_id": "64ba1614-82e8-476f-957d-a29198c7a26e", "openfda": {"unii": ["9WP59609J6"], "rxcui": ["1730076", "1730078"], "spl_set_id": ["5831e15a-3efa-48bb-9d49-8451f78d9868"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 CARTON (65219-130-02)  / 2 mL in 1 VIAL (65219-130-01)", "package_ndc": "65219-130-02", "marketing_start_date": "20250215"}], "brand_name": "CHLORPROMAZINE HYDROCHLORIDE", "product_id": "65219-130_64ba1614-82e8-476f-957d-a29198c7a26e", "dosage_form": "INJECTION", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "65219-130", "generic_name": "CHLORPROMAZINE HYDROCHLORIDE", "labeler_name": "Fresenius Kabi USA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CHLORPROMAZINE HYDROCHLORIDE", "active_ingredients": [{"name": "CHLORPROMAZINE HYDROCHLORIDE", "strength": "25 mg/mL"}], "application_number": "ANDA216724", "marketing_category": "ANDA", "marketing_start_date": "20250215", "listing_expiration_date": "20261231"}