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 ID69263-822_7cc3db74-121d-6e9f-e053-2a91aa0a0739
NDC69263-822
Product TypeHuman Prescription Drug
Proprietary NameBeta 1 Kit
Generic NameBetamethasone Sodium Phosphate, Betamethasone Acetate
Dosage FormKit
Route of AdministrationINTRA-ARTICULAR; INTRALESIONAL; INTRAMUSCULAR
Marketing Start Date2015-08-25
Marketing CategoryANDA / ANDA
Application NumberANDA090747
Labeler NameOaklock, LLC
Active Ingredient Strength0
NDC Exclude FlagN
Listing Certified Through2019-12-31

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 Date2015-08-25
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 69263-822-01 [69263082201]

Beta 1 Kit KIT
Marketing CategoryANDA
Application NumberANDA090747
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2015-08-25

Drug Details

OpenFDA Data

SPL SET ID:7e63c73d-30b2-4f47-a817-0313a08281c1
Manufacturer
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"

    NDCBrand NameGeneric Name
    69263-822Beta 1 KitBetamethasone Sodium Phosphate, Betamethasone Acetate
    69263-805BSP 0820Betamethasone Sodium Phosphate, Betamethasone Acetate

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