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"60722-5011-1" National Drug Code (NDC)
Prednisolone 1000 TABLET in 1 BOTTLE (60722-5011-1)
(Zhejiang Xianju Pharmaceutical Co., Ltd.)
NDC Code
60722-5011-1
Package Description
1000 TABLET in 1 BOTTLE (60722-5011-1)
Product NDC
60722-5011
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Prednisolone
Non-Proprietary Name
Prednisolone
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20240901
Marketing Category Name
ANDA
Application Number
ANDA218083
Manufacturer
Zhejiang Xianju Pharmaceutical Co., Ltd.
Substance Name
PREDNISOLONE
Strength
5
Strength Unit
mg/1
Pharmacy Classes
Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/60722-5011-1