chloroprocaine hydrochloride

Generic: chloroprocaine hydrochloride

Labeler: hikma pharmaceuticals usa inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name chloroprocaine hydrochloride
Generic Name chloroprocaine hydrochloride
Labeler hikma pharmaceuticals usa inc.
Dosage Form INJECTION, SOLUTION
Routes
EPIDURAL INFILTRATION INTRACAUDAL PERINEURAL
Active Ingredients

chloroprocaine hydrochloride 30 mg/mL

Manufacturer
Hikma Pharmaceuticals USA Inc.

Identifiers & Regulatory

Product NDC 0143-9210
Product ID 0143-9210_a652f290-f8c6-4483-9fe4-b1fd50dec37d
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA040273
Listing Expiration 2026-12-31
Marketing Start 1998-11-01

Pharmacologic Class

Classes
ester local anesthetic [epc] esters [cs] local anesthesia [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 01439210
Hyphenated Format 0143-9210

Supplemental Identifiers

RxCUI
992809 1794184
UNII
LT7Z1YW11H

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 chloroprocaine hydrochloride (source: ndc)
Generic Name chloroprocaine hydrochloride (source: ndc)
Application Number ANDA040273 (source: ndc)
Routes
EPIDURAL INFILTRATION INTRACAUDAL PERINEURAL
source: ndc

Resolved Composition

Strengths
  • 30 mg/mL
source: ndc
Packaging
  • 10 VIAL in 1 CARTON (0143-9210-10) / 20 mL in 1 VIAL (0143-9210-01)
source: ndc

Packages (1)

0143-9210-10 10 VIAL in 1 CARTON (0143-9210-10) / 20 mL in 1 VIAL (0143-9210-01)

Ingredients (1)

chloroprocaine hydrochloride (30 mg/mL)

Linked Drug Pages (1)

Chloroprocaine Hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["EPIDURAL", "INFILTRATION", "INTRACAUDAL", "PERINEURAL"], "spl_id": "a652f290-f8c6-4483-9fe4-b1fd50dec37d", "openfda": {"unii": ["LT7Z1YW11H"], "rxcui": ["992809", "1794184"], "spl_set_id": ["e21e24d5-0535-4962-b9ed-7957fe4ed3db"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 CARTON (0143-9210-10)  / 20 mL in 1 VIAL (0143-9210-01)", "package_ndc": "0143-9210-10", "marketing_start_date": "19981101"}], "brand_name": "Chloroprocaine Hydrochloride", "product_id": "0143-9210_a652f290-f8c6-4483-9fe4-b1fd50dec37d", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Ester Local Anesthetic [EPC]", "Esters [CS]", "Local Anesthesia [PE]"], "product_ndc": "0143-9210", "generic_name": "Chloroprocaine Hydrochloride", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Chloroprocaine Hydrochloride", "active_ingredients": [{"name": "CHLOROPROCAINE HYDROCHLORIDE", "strength": "30 mg/mL"}], "application_number": "ANDA040273", "marketing_category": "ANDA", "marketing_start_date": "19981101", "listing_expiration_date": "20261231"}