"68382-034-10" National Drug Code (NDC)

Venlafaxine Hydrochloride 1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68382-034-10)
(Zydus Pharmaceuticals USA Inc.)

NDC Code68382-034-10
Package Description1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68382-034-10)
Product NDC68382-034
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameVenlafaxine Hydrochloride
Non-Proprietary NameVenlafaxine Hydrochloride
Dosage FormCAPSULE, EXTENDED RELEASE
UsageORAL
Start Marketing Date20110601
Marketing Category NameANDA
Application NumberANDA090174
ManufacturerZydus Pharmaceuticals USA Inc.
Substance NameVENLAFAXINE HYDROCHLORIDE
Strength37.5
Strength Unitmg/1
Pharmacy ClassesNorepinephrine Uptake Inhibitors [MoA], Serotonin Uptake Inhibitors [MoA], Serotonin and Norepinephrine Reuptake Inhibitor [EPC]

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