ketamine hydrochloride

Generic: ketamine hydrochloride

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

Drug Facts

Product Profile

Brand Name ketamine hydrochloride
Generic Name ketamine hydrochloride
Labeler henry schein, inc.
Dosage Form INJECTION, SOLUTION, CONCENTRATE
Routes
INTRAMUSCULAR INTRAVENOUS
Active Ingredients

ketamine hydrochloride 50 mg/mL

Manufacturer
Henry Schein, Inc.

Identifiers & Regulatory

Product NDC 0404-9882
Product ID 0404-9882_fb0436cf-9ef7-4b0b-8c47-8068ffc0bbf9
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA074549
DEA Schedule ciii
Listing Expiration 2026-12-31
Marketing Start 2022-01-11

Pharmacologic Class

Classes
general anesthesia [pe] general anesthetic [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 04049882
Hyphenated Format 0404-9882

Supplemental Identifiers

RxCUI
238084
UNII
O18YUO0I83

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 ketamine hydrochloride (source: ndc)
Generic Name ketamine hydrochloride (source: ndc)
Application Number ANDA074549 (source: ndc)
Routes
INTRAMUSCULAR INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 50 mg/mL
source: ndc
Packaging
  • 1 VIAL in 1 BAG (0404-9882-10) / 10 mL in 1 VIAL
source: ndc

Packages (1)

0404-9882-10 1 VIAL in 1 BAG (0404-9882-10) / 10 mL in 1 VIAL

Ingredients (1)

ketamine hydrochloride (50 mg/mL)

Linked Drug Pages (1)

KETAMINE HYDROCHLORIDE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "fb0436cf-9ef7-4b0b-8c47-8068ffc0bbf9", "openfda": {"unii": ["O18YUO0I83"], "rxcui": ["238084"], "spl_set_id": ["dd8eff00-b92e-4f48-8b57-0464484d6ddf"], "manufacturer_name": ["Henry Schein, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 BAG (0404-9882-10)  / 10 mL in 1 VIAL", "package_ndc": "0404-9882-10", "marketing_start_date": "20220111"}], "brand_name": "KETAMINE HYDROCHLORIDE", "product_id": "0404-9882_fb0436cf-9ef7-4b0b-8c47-8068ffc0bbf9", "dosage_form": "INJECTION, SOLUTION, CONCENTRATE", "pharm_class": ["General Anesthesia [PE]", "General Anesthetic [EPC]"], "product_ndc": "0404-9882", "dea_schedule": "CIII", "generic_name": "ketamine hydrochloride", "labeler_name": "Henry Schein, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "KETAMINE HYDROCHLORIDE", "active_ingredients": [{"name": "KETAMINE HYDROCHLORIDE", "strength": "50 mg/mL"}], "application_number": "ANDA074549", "marketing_category": "ANDA", "marketing_start_date": "20220111", "listing_expiration_date": "20261231"}