"67046-852-21" National Drug Code (NDC)

Venlafaxine 21 TABLET in 1 BLISTER PACK (67046-852-21)
(Contract Pharmacy Services-PA)

NDC Code67046-852-21
Package Description21 TABLET in 1 BLISTER PACK (67046-852-21)
Product NDC67046-852
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameVenlafaxine
Non-Proprietary NameVenlafaxine
Dosage FormTABLET
UsageORAL
Start Marketing Date20170921
Marketing Category NameANDA
Application NumberANDA078554
ManufacturerContract Pharmacy Services-PA
Substance NameVENLAFAXINE HYDROCHLORIDE
Strength75
Strength Unitmg/1
Pharmacy ClassesNorepinephrine Uptake Inhibitors [MoA],Serotonin and Norepinephrine Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]

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