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"68084-715-32" National Drug Code (NDC)

Fenofibric Acid 20 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-715-32) > 1 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (68084-715-33)
(American Health Packaging)

NDC Code68084-715-32
Package Description20 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-715-32) > 1 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (68084-715-33)
Product NDC68084-715
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFenofibric Acid
Proprietary Name SuffixDelayed-release
Non-Proprietary NameFenofibric Acid
Dosage FormCAPSULE, DELAYED RELEASE
UsageORAL
Start Marketing Date20150215
Marketing Category NameANDA
Application NumberANDA201573
ManufacturerAmerican Health Packaging
Substance NameCHOLINE FENOFIBRATE
Strength135
Strength Unitmg/1
Pharmacy ClassesPeroxisome Proliferator Receptor alpha Agonist [EPC],Peroxisome Proliferator-activated Receptor alpha Agonists [MoA],PPAR alpha [Chemical/Ingredient]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/68084-715-32





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