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"0093-7256-52" National Drug Code (NDC)

Glimepiride 250 TABLET in 1 BOTTLE (0093-7256-52)
(Teva Pharmaceuticals USA, Inc.)

NDC Code0093-7256-52
Package Description250 TABLET in 1 BOTTLE (0093-7256-52)
Product NDC0093-7256
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameGlimepiride
Non-Proprietary NameGlimepiride
Dosage FormTABLET
UsageORAL
Start Marketing Date20051006
End Marketing Date20200831
Marketing Category NameANDA
Application NumberANDA076802
ManufacturerTeva Pharmaceuticals USA, Inc.
Substance NameGLIMEPIRIDE
Strength4
Strength Unitmg/1
Pharmacy ClassesSulfonylurea [EPC],Sulfonylurea Compounds [CS]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/0093-7256-52





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