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"69844-022-03" National Drug Code (NDC)

Fenofibric Acid Delayed-release 1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (69844-022-03)
(Graviti Pharmaceuticals Private Limited)

NDC Code69844-022-03
Package Description1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (69844-022-03)
Product NDC69844-022
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFenofibric Acid Delayed-release
Non-Proprietary NameFenofibric Acid
Dosage FormCAPSULE, DELAYED RELEASE
UsageORAL
Start Marketing Date20190718
Marketing Category NameANDA
Application NumberANDA211626
ManufacturerGraviti Pharmaceuticals Private Limited
Substance NameFENOFIBRIC ACID
Strength45
Strength Unitmg/1
Pharmacy ClassesPeroxisome Proliferator Receptor alpha Agonist [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/69844-022-03





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