"71921-216-01" National Drug Code (NDC)

Glimepiride 100 TABLET in 1 BOTTLE (71921-216-01)
(Florida Pharmaceutical Products, LLC)

NDC Code71921-216-01
Package Description100 TABLET in 1 BOTTLE (71921-216-01)
Product NDC71921-216
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameGlimepiride
Non-Proprietary NameGlimepiride
Dosage FormTABLET
UsageORAL
Start Marketing Date20230731
Marketing Category NameANDA
Application NumberANDA202112
ManufacturerFlorida Pharmaceutical Products, LLC
Substance NameGLIMEPIRIDE
Strength4
Strength Unitmg/1
Pharmacy ClassesSulfonylurea Compounds [CS], Sulfonylurea [EPC]

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