NDC 69263-820

Pro-C-Dure 5 Kit

Kenalog

Pro-C-Dure 5 Kit is a Intra-articular; Intramuscular Kit in the Human Prescription Drug category. It is labeled and distributed by Oaklock, Llc. The primary component is .

Product ID69263-820_5df51313-ffe3-edd4-e053-2991aa0ab928
NDC69263-820
Product TypeHuman Prescription Drug
Proprietary NamePro-C-Dure 5 Kit
Generic NameKenalog
Dosage FormKit
Route of AdministrationINTRA-ARTICULAR; INTRAMUSCULAR
Marketing Start Date2015-08-17
Marketing CategoryNDA / NDA
Application NumberNDA014901
Labeler NameOaklock, LLC
Active Ingredient Strength0
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 69263-820-01

1 KIT in 1 CARTON (69263-820-01) * 1 VIAL, SINGLE-DOSE in 1 CARTON (0003-0293-05) > 1 mL in 1 VIAL, SINGLE-DOSE
Marketing Start Date2015-08-17
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 69263-820-01 [69263082001]

Pro-C-Dure 5 Kit KIT
Marketing CategoryNDA
Application NumberNDA014901
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2015-08-17
Inactivation Date2020-01-31
Reactivation Date2020-03-11

Drug Details

OpenFDA Data

SPL SET ID:68fc4863-595a-48f2-809b-98425d9607f4
Manufacturer
RxNorm Concept Unique ID - RxCUI
  • 1085754
  • 1085756
  • NDC Crossover Matching brand name "Pro-C-Dure 5 Kit" or generic name "Kenalog"

    NDCBrand NameGeneric Name
    69263-820Pro-C-Dure 5 Kitkenalog
    69263-821Pro-C-Dure 6 Kitkenalog

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