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"59651-333-05" National Drug Code (NDC)
Albuterol 500 TABLET in 1 BOTTLE (59651-333-05)
(Aurobindo Pharma Limited)
NDC Code
59651-333-05
Package Description
500 TABLET in 1 BOTTLE (59651-333-05)
Product NDC
59651-333
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Albuterol
Non-Proprietary Name
Albuterol
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20200514
Marketing Category Name
ANDA
Application Number
ANDA213657
Manufacturer
Aurobindo Pharma Limited
Substance Name
ALBUTEROL SULFATE
Strength
2
Strength Unit
mg/1
Pharmacy Classes
Adrenergic beta2-Agonists [MoA], beta2-Adrenergic Agonist [EPC]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/59651-333-05