chlorpromazine hydrochloride

Generic: chlorpromazine hydrochloride

Labeler: devatis, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name chlorpromazine hydrochloride
Generic Name chlorpromazine hydrochloride
Labeler devatis, inc.
Dosage Form INJECTION
Routes
INTRAMUSCULAR
Active Ingredients

chlorpromazine hydrochloride 25 mg/mL

Manufacturer
Devatis, Inc.

Identifiers & Regulatory

Product NDC 73043-048
Product ID 73043-048_4635d706-5e3d-4817-bf04-802a20f72a70
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA218229
Listing Expiration 2026-12-31
Marketing Start 2024-11-01

Pharmacologic Class

Classes
phenothiazine [epc] phenothiazines [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 73043048
Hyphenated Format 73043-048

Supplemental Identifiers

RxCUI
1730076 1730078
UPC
0373043048255 0373043049252
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 ANDA218229 (source: ndc)
Routes
INTRAMUSCULAR
source: ndc

Resolved Composition

Strengths
  • 25 mg/mL
source: ndc
Packaging
  • 25 AMPULE in 1 CARTON (73043-048-25) / 1 mL in 1 AMPULE (73043-048-01)
source: ndc

Packages (1)

73043-048-25 25 AMPULE in 1 CARTON (73043-048-25) / 1 mL in 1 AMPULE (73043-048-01)

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": "4635d706-5e3d-4817-bf04-802a20f72a70", "openfda": {"upc": ["0373043048255", "0373043049252"], "unii": ["9WP59609J6"], "rxcui": ["1730076", "1730078"], "spl_set_id": ["b73b9044-7132-41b7-83d4-2d135ea831f1"], "manufacturer_name": ["Devatis, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 AMPULE in 1 CARTON (73043-048-25)  / 1 mL in 1 AMPULE (73043-048-01)", "package_ndc": "73043-048-25", "marketing_start_date": "20241101"}], "brand_name": "Chlorpromazine hydrochloride", "product_id": "73043-048_4635d706-5e3d-4817-bf04-802a20f72a70", "dosage_form": "INJECTION", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "73043-048", "generic_name": "Chlorpromazine hydrochloride", "labeler_name": "Devatis, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Chlorpromazine hydrochloride", "active_ingredients": [{"name": "CHLORPROMAZINE HYDROCHLORIDE", "strength": "25 mg/mL"}], "application_number": "ANDA218229", "marketing_category": "ANDA", "marketing_start_date": "20241101", "listing_expiration_date": "20261231"}