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"61919-250-04" National Drug Code (NDC)
Glimepiride 4 TABLET in 1 BOTTLE (61919-250-04)
(DIRECT RX)
NDC Code
61919-250-04
Package Description
4 TABLET in 1 BOTTLE (61919-250-04)
Product NDC
61919-250
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Glimepiride
Non-Proprietary Name
Glimepiride
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20160204
Marketing Category Name
ANDA
Application Number
ANDA078181
Manufacturer
DIRECT RX
Substance Name
GLIMEPIRIDE
Strength
4
Strength Unit
mg/1
Pharmacy Classes
Sulfonylurea Compounds [CS], Sulfonylurea [EPC]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/61919-250-04