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"69263-822-01" National Drug Code (NDC)
Beta 1 Kit 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
(Oaklock, LLC)
NDC Code
69263-822-01
Package Description
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
Product NDC
69263-822
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Beta 1 Kit
Non-Proprietary Name
Betamethasone Sodium Phosphate, Betamethasone Acetate
Dosage Form
KIT
Usage
INTRA-ARTICULAR; INTRALESIONAL; INTRAMUSCULAR
Start Marketing Date
20150825
Marketing Category Name
ANDA
Application Number
ANDA090747
Manufacturer
Oaklock, LLC
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/69263-822-01