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"61919-291-37" National Drug Code (NDC)
Prednisolone 240 mL in 1 BOTTLE (61919-291-37)
(DIRECT RX)
NDC Code
61919-291-37
Package Description
240 mL in 1 BOTTLE (61919-291-37)
Product NDC
61919-291
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Prednisolone
Non-Proprietary Name
Prednisolone
Dosage Form
SOLUTION
Usage
ORAL
Start Marketing Date
20140101
Marketing Category Name
ANDA
Application Number
ANDA040401
Manufacturer
DIRECT RX
Substance Name
PREDNISOLONE
Strength
15
Strength Unit
mg/5mL
Pharmacy Classes
Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/61919-291-37