ketamine hydrochloride

Generic: ketamine hydrochloride

Labeler: baxter healthcare corporation
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name ketamine hydrochloride
Generic Name ketamine hydrochloride
Labeler baxter healthcare corporation
Dosage Form INJECTION
Routes
INTRAMUSCULAR INTRAVENOUS
Active Ingredients

ketamine hydrochloride 10 mg/mL

Manufacturer
Baxter Healthcare Corporation

Identifiers & Regulatory

Product NDC 43066-177
Product ID 43066-177_549d6ed3-3c9b-4ea2-8aaf-f61d43e04602
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA219684
DEA Schedule ciii
Listing Expiration 2026-12-31
Marketing Start 2025-09-17

Pharmacologic Class

Classes
general anesthesia [pe] general anesthetic [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 43066177
Hyphenated Format 43066-177

Supplemental Identifiers

RxCUI
2723913
UNII
O18YUO0I83

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 ketamine hydrochloride (source: ndc)
Generic Name ketamine hydrochloride (source: ndc)
Application Number ANDA219684 (source: ndc)
Routes
INTRAMUSCULAR INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 10 mg/mL
source: ndc
Packaging
  • 5 CARTON in 1 CARTON (43066-177-05) / 1 SYRINGE, PLASTIC in 1 CARTON (43066-177-01) / 10 mL in 1 SYRINGE, PLASTIC
source: ndc

Packages (1)

43066-177-05 5 CARTON in 1 CARTON (43066-177-05) / 1 SYRINGE, PLASTIC in 1 CARTON (43066-177-01) / 10 mL in 1 SYRINGE, PLASTIC

Ingredients (1)

ketamine hydrochloride (10 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": "549d6ed3-3c9b-4ea2-8aaf-f61d43e04602", "openfda": {"unii": ["O18YUO0I83"], "rxcui": ["2723913"], "spl_set_id": ["549d6ed3-3c9b-4ea2-8aaf-f61d43e04602"], "manufacturer_name": ["Baxter Healthcare Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "5 CARTON in 1 CARTON (43066-177-05)  / 1 SYRINGE, PLASTIC in 1 CARTON (43066-177-01)  / 10 mL in 1 SYRINGE, PLASTIC", "package_ndc": "43066-177-05", "marketing_start_date": "20250917"}], "brand_name": "KETAMINE HYDROCHLORIDE", "product_id": "43066-177_549d6ed3-3c9b-4ea2-8aaf-f61d43e04602", "dosage_form": "INJECTION", "pharm_class": ["General Anesthesia [PE]", "General Anesthetic [EPC]"], "product_ndc": "43066-177", "dea_schedule": "CIII", "generic_name": "KETAMINE HYDROCHLORIDE", "labeler_name": "Baxter Healthcare Corporation", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "KETAMINE HYDROCHLORIDE", "active_ingredients": [{"name": "KETAMINE HYDROCHLORIDE", "strength": "10 mg/mL"}], "application_number": "ANDA219684", "marketing_category": "ANDA", "marketing_start_date": "20250917", "listing_expiration_date": "20261231"}