chlorpromazine hci

Generic: chlorpromazine hci

Labeler: hf acquisition co llc, dba healthfirst
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name chlorpromazine hci
Generic Name chlorpromazine hci
Labeler hf acquisition co llc, dba healthfirst
Dosage Form INJECTION
Routes
INTRAMUSCULAR
Active Ingredients

chlorpromazine hydrochloride 25 mg/mL

Manufacturer
HF Acquisition Co LLC, DBA HealthFirst

Identifiers & Regulatory

Product NDC 51662-1406
Product ID 51662-1406_2b37c8a2-d5d6-015f-e063-6394a90a3899
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA083329
Listing Expiration 2026-12-31
Marketing Start 2019-10-21

Pharmacologic Class

Classes
phenothiazine [epc] phenothiazines [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 516621406
Hyphenated Format 51662-1406

Supplemental Identifiers

RxCUI
1730076
UNII
9WP59609J6

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 ANDA083329 (source: ndc)
Routes
INTRAMUSCULAR
source: ndc

Resolved Composition

Strengths
  • 25 mg/mL
source: ndc
Packaging
  • 2 mL in 1 AMPULE (51662-1406-1)
source: ndc

Packages (1)

51662-1406-1 2 mL in 1 AMPULE (51662-1406-1)

Ingredients (1)

chlorpromazine hydrochloride (25 mg/mL)

Linked Drug Pages (1)

CHLORPROMAZINE HCI ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAMUSCULAR"], "spl_id": "2b37c8a2-d5d6-015f-e063-6394a90a3899", "openfda": {"unii": ["9WP59609J6"], "rxcui": ["1730076"], "spl_set_id": ["9575c766-3758-6f33-e053-2995a90ae6b1"], "manufacturer_name": ["HF Acquisition Co LLC, DBA HealthFirst"]}, "finished": true, "packaging": [{"sample": false, "description": "2 mL in 1 AMPULE (51662-1406-1)", "package_ndc": "51662-1406-1", "marketing_start_date": "20191021"}], "brand_name": "CHLORPROMAZINE HCI", "product_id": "51662-1406_2b37c8a2-d5d6-015f-e063-6394a90a3899", "dosage_form": "INJECTION", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "51662-1406", "generic_name": "CHLORPROMAZINE HCI", "labeler_name": "HF Acquisition Co LLC, DBA HealthFirst", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CHLORPROMAZINE HCI", "active_ingredients": [{"name": "CHLORPROMAZINE HYDROCHLORIDE", "strength": "25 mg/mL"}], "application_number": "ANDA083329", "marketing_category": "ANDA", "marketing_start_date": "20191021", "listing_expiration_date": "20261231"}