Package 43066-177-05
Brand: ketamine hydrochloride
Generic: ketamine hydrochloridePackage Facts
Identity
Package NDC
43066-177-05
Digits Only
4306617705
Product NDC
43066-177
Description
5 CARTON in 1 CARTON (43066-177-05) / 1 SYRINGE, PLASTIC in 1 CARTON (43066-177-01) / 10 mL in 1 SYRINGE, PLASTIC
Marketing
Marketing Status
Brand
ketamine hydrochloride
Generic
ketamine hydrochloride
Sample Package
No
Linked Drug Pages (1)
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"}