"55111-322-30" National Drug Code (NDC)

Glimepiride 30 TABLET in 1 BOTTLE (55111-322-30)
(Dr. Reddy's Laboratories Limited)

NDC Code55111-322-30
Package Description30 TABLET in 1 BOTTLE (55111-322-30)
Product NDC55111-322
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameGlimepiride
Non-Proprietary NameGlimepiride
Dosage FormTABLET
UsageORAL
Start Marketing Date20051006
Marketing Category NameANDA
Application NumberANDA077091
ManufacturerDr. Reddy's Laboratories Limited
Substance NameGLIMEPIRIDE
Strength4
Strength Unitmg/1
Pharmacy ClassesSulfonylurea Compounds [CS], Sulfonylurea [EPC]

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