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"70985-019-03" National Drug Code (NDC)
Venlafaxine Hydrochloride 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (70985-019-03)
(Drug Ocean LLC)
NDC Code
70985-019-03
Package Description
30 TABLET, EXTENDED RELEASE in 1 BOTTLE (70985-019-03)
Product NDC
70985-019
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Venlafaxine Hydrochloride
Non-Proprietary Name
Venlafaxine
Dosage Form
TABLET, EXTENDED RELEASE
Usage
ORAL
Start Marketing Date
20231005
Marketing Category Name
ANDA
Application Number
ANDA216044
Manufacturer
Drug Ocean LLC
Substance Name
VENLAFAXINE HYDROCHLORIDE
Strength
75
Strength Unit
mg/1
Pharmacy Classes
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/70985-019-03