chlorpromazine hydrochloride

Generic: chlorpromazine hydrochloride

Labeler: eugia us llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name chlorpromazine hydrochloride
Generic Name chlorpromazine hydrochloride
Labeler eugia us llc
Dosage Form INJECTION
Routes
INTRAMUSCULAR
Active Ingredients

chlorpromazine hydrochloride 25 mg/mL

Manufacturer
Eugia US LLC

Identifiers & Regulatory

Product NDC 55150-318
Product ID 55150-318_de29daf4-7c8a-4b37-b33c-e9f34f3a14c7
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA211816
Listing Expiration 2026-12-31
Marketing Start 2020-07-07

Pharmacologic Class

Classes
phenothiazine [epc] phenothiazines [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 55150318
Hyphenated Format 55150-318

Supplemental Identifiers

RxCUI
1730076 1730078
UPC
0355150319251
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 ANDA211816 (source: ndc)
Routes
INTRAMUSCULAR
source: ndc

Resolved Composition

Strengths
  • 25 mg/mL
source: ndc
Packaging
  • 25 AMPULE in 1 CARTON (55150-318-25) / 1 mL in 1 AMPULE (55150-318-01)
source: ndc

Packages (1)

Ingredients (1)

chlorpromazine hydrochloride (25 mg/mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR"], "spl_id": "de29daf4-7c8a-4b37-b33c-e9f34f3a14c7", "openfda": {"upc": ["0355150319251"], "unii": ["9WP59609J6"], "rxcui": ["1730076", "1730078"], "spl_set_id": ["07e6144a-b460-4887-b8e2-dd371c14a55c"], "manufacturer_name": ["Eugia US LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 AMPULE in 1 CARTON (55150-318-25)  / 1 mL in 1 AMPULE (55150-318-01)", "package_ndc": "55150-318-25", "marketing_start_date": "20200707"}], "brand_name": "CHLORPROMAZINE HYDROCHLORIDE", "product_id": "55150-318_de29daf4-7c8a-4b37-b33c-e9f34f3a14c7", "dosage_form": "INJECTION", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "55150-318", "generic_name": "CHLORPROMAZINE HYDROCHLORIDE", "labeler_name": "Eugia US LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CHLORPROMAZINE HYDROCHLORIDE", "active_ingredients": [{"name": "CHLORPROMAZINE HYDROCHLORIDE", "strength": "25 mg/mL"}], "application_number": "ANDA211816", "marketing_category": "ANDA", "marketing_start_date": "20200707", "listing_expiration_date": "20261231"}