NDC 69263-822

Beta 1 Kit

Betamethasone Sodium Phosphate, Betamethasone Acetate

Beta 1 Kit is a Intra-articular; Intralesional; Intramuscular Kit in the Human Prescription Drug category. It is labeled and distributed by Oaklock, Llc. The primary component is .

• Product ID: 69263-822_7cc3db74-121d-6e9f-e053-2a91aa0a0739
• NDC: 69263-822
• Product Type: Human Prescription Drug
• Proprietary Name: Beta 1 Kit
• Generic Name: Betamethasone Sodium Phosphate, Betamethasone Acetate
• Dosage Form: Kit
• Route of Administration: INTRA-ARTICULAR; INTRALESIONAL; INTRAMUSCULAR
• Marketing Start Date: 2015-08-25
• Marketing Category: ANDA / ANDA
• Application Number: ANDA090747
• Labeler Name: Oaklock, LLC
• Active Ingredient Strength: 0
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 69263-822-01

1 KIT in 1 CARTON (69263-822-01) * 1 VIAL, MULTI-DOSE in 1 CARTON (0517-0720-01) > 5 mL in 1 VIAL, MULTI-DOSE

• Marketing Start Date: 2015-08-25
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 69263-822-01 [69263082201]

Beta 1 Kit KIT

• Marketing Category: ANDA
• Application Number: ANDA090747
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2015-08-25

Drug Details

OpenFDA Data

• SPL SET ID: 7e63c73d-30b2-4f47-a817-0313a08281c1
• Manufacturer:
  • Oaklock, LLC
• RxNorm Concept Unique ID - RxCUI:
  • 578803
• UPC Code:
  • 0069263822019

NDC Crossover Matching brand name "Beta 1 Kit" or generic name "Betamethasone Sodium Phosphate, Betamethasone Acetate"

NDC	Brand Name	Generic Name
69263-822	Beta 1 Kit	Betamethasone Sodium Phosphate, Betamethasone Acetate
69263-805	BSP 0820	Betamethasone Sodium Phosphate, Betamethasone Acetate