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"16571-100-10" National Drug Code (NDC)
Montelukast Sodium 1000 TABLET in 1 BOTTLE (16571-100-10)
(Rising Pharma Holdings, Inc.)
NDC Code
16571-100-10
Package Description
1000 TABLET in 1 BOTTLE (16571-100-10)
Product NDC
16571-100
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Montelukast Sodium
Non-Proprietary Name
Montelukast Sodium
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20230601
Marketing Category Name
ANDA
Application Number
ANDA209012
Manufacturer
Rising Pharma Holdings, Inc.
Substance Name
MONTELUKAST SODIUM
Strength
10
Strength Unit
mg/1
Pharmacy Classes
Leukotriene Receptor Antagonist [EPC], Leukotriene Receptor Antagonists [MoA]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/16571-100-10