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

"60687-655-21" National Drug Code (NDC)

Fenofibrate 30 BLISTER PACK in 1 CARTON (60687-655-21) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-655-11)
(American Health Packaging)

NDC Code60687-655-21
Package Description30 BLISTER PACK in 1 CARTON (60687-655-21) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-655-11)
Product NDC60687-655
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFenofibrate
Non-Proprietary NameFenofibrate
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20221202
End Marketing Date20240731
Marketing Category NameANDA
Application NumberANDA076635
ManufacturerAmerican Health Packaging
Substance NameFENOFIBRATE
Strength54
Strength Unitmg/1
Pharmacy ClassesPeroxisome Proliferator Receptor alpha Agonist [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/60687-655-21





Copyright © 2007-2024 www.ndcvalidator.com