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"70771-1312-5" National Drug Code (NDC)

Desvenlafaxine 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1312-5)
(Zydus Lifesciences Limited)

NDC Code70771-1312-5
Package Description500 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1312-5)
Product NDC70771-1312
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameDesvenlafaxine
Non-Proprietary NameDesvenlafaxine
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20180508
Marketing Category NameANDA
Application NumberANDA204020
ManufacturerZydus Lifesciences Limited
Substance NameDESVENLAFAXINE
Strength100
Strength Unitmg/1
Pharmacy ClassesCytochrome P450 2D6 Inhibitors [MoA], Norepinephrine Uptake Inhibitors [MoA], Serotonin Uptake Inhibitors [MoA], Serotonin and Norepinephrine Reuptake Inhibitor [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/70771-1312-5





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