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"68180-129-02" National Drug Code (NDC)

Fenofibric Acid 500 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68180-129-02)
(Lupin Pharmaceuticals, Inc.)

NDC Code68180-129-02
Package Description500 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68180-129-02)
Product NDC68180-129
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFenofibric Acid
Non-Proprietary NameFenofibric Acid
Dosage FormCAPSULE, DELAYED RELEASE
UsageORAL
Start Marketing Date20131204
Marketing Category NameANDA
Application NumberANDA200750
ManufacturerLupin Pharmaceuticals, Inc.
Substance NameCHOLINE FENOFIBRATE
Strength135
Strength Unitmg/1
Pharmacy ClassesPeroxisome Proliferator Receptor alpha Agonist [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/68180-129-02





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