"69263-820-01" National Drug Code (NDC)

NDC Code	69263-820-01
Package Description	*1 KIT in 1 CARTON (69263-820-01) 1 VIAL in 1 CARTON (70121-1049-2) / 1 mL in 1 VIAL**
Product NDC	69263-820
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Pro-c-dure 5 Kit
Non-Proprietary Name	Kenalog
Dosage Form	KIT
Usage	INTRA-ARTICULAR; INTRAMUSCULAR
Start Marketing Date	20211004
Marketing Category Name	UNAPPROVED DRUG OTHER
Manufacturer	Oaklock, LLC