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"71921-216-50" National Drug Code (NDC)

Glimepiride 500 TABLET in 1 BOTTLE (71921-216-50)
(Florida Pharmaceutical Products, LLC)

NDC Code71921-216-50
Package Description500 TABLET in 1 BOTTLE (71921-216-50)
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]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/71921-216-50





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