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"53489-177-05" National Drug Code (NDC)
Albuterol Sulfate 500 TABLET in 1 BOTTLE (53489-177-05)
(Sun Pharmaceutical Industries, Inc.)
NDC Code
53489-177-05
Package Description
500 TABLET in 1 BOTTLE (53489-177-05)
Product NDC
53489-177
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Albuterol Sulfate
Non-Proprietary Name
Albuterol Sulfate
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
19891205
Marketing Category Name
ANDA
Application Number
ANDA072637
Manufacturer
Sun Pharmaceutical Industries, Inc.
Substance Name
ALBUTEROL SULFATE
Strength
4
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/53489-177-05