www.ndcvalidator.com
National Drug Code Lookup | NDC Directory | About | Feedback

"59762-0737-5" National Drug Code (NDC)

Gemfibrozil 500 TABLET, FILM COATED in 1 BOTTLE (59762-0737-5)
(Greenstone LLC)

NDC Code59762-0737-5
Package Description500 TABLET, FILM COATED in 1 BOTTLE (59762-0737-5)
Product NDC59762-0737
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameGemfibrozil
Non-Proprietary NameGemfibrozil
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20201118
End Marketing Date20220831
Marketing Category NameNDA AUTHORIZED GENERIC
Application NumberNDA018422
ManufacturerGreenstone LLC
Substance NameGEMFIBROZIL
Strength600
Strength Unitmg/1
Pharmacy ClassesPPAR alpha [CS], Peroxisome Proliferator Receptor alpha Agonist [EPC], Peroxisome Proliferator-activated Receptor alpha Agonists [MoA]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/59762-0737-5





Copyright © 2007-2024 www.ndcvalidator.com