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 ID: 69263-820_5df51313-ffe3-edd4-e053-2991aa0ab928
• NDC: 69263-820
• Product Type: Human Prescription Drug
• Proprietary Name: Pro-C-Dure 5 Kit
• Generic Name: Kenalog
• Dosage Form: Kit
• Route of Administration: INTRA-ARTICULAR; INTRAMUSCULAR
• Marketing Start Date: 2015-08-17
• Marketing Category: NDA / NDA
• Application Number: NDA014901
• Labeler Name: Oaklock, LLC
• Active Ingredient Strength: 0
• NDC Exclude Flag: E
• Listing Certified Through: 2018-12-31

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 Date: 2015-08-17
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 69263-820-01 [69263082001]

Pro-C-Dure 5 Kit KIT

• Marketing Category: NDA
• Application Number: NDA014901
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2015-08-17
• Inactivation Date: 2020-01-31
• Reactivation Date: 2020-03-11

Drug Details

OpenFDA Data

• SPL SET ID: 68fc4863-595a-48f2-809b-98425d9607f4
• Manufacturer:
  • Oaklock, LLC
• RxNorm Concept Unique ID - RxCUI:
  • 1085754
  • 1085756

NDC Crossover Matching brand name "Pro-C-Dure 5 Kit" or generic name "Kenalog"

NDC	Brand Name	Generic Name
69263-820	Pro-C-Dure 5 Kit	kenalog
69263-821	Pro-C-Dure 6 Kit	kenalog