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Venlafaxine Hydrochloride - Venlafaxine Hydrochloride

Navigation: NDC > Supplier starting with: S > SUN PHARMA GLOBAL INC.
Field Value
NDC Code: 41616-759
Proprietary Name: Venlafaxine Hydrochloride
Suffix:
Non-Proprietary Name: Venlafaxine Hydrochloride
Dosage Form: TABLET, EXTENDED RELEASE
Method: ORAL
Original Marketing Date: 18-08-2010
Category Name: ANDA
Application Number: ANDA091272
Labeler: SUN PHARMA GLOBAL INC.
Substance Name: VENLAFAXINE HYDROCHLORIDE
Active Numerator Strength: 75
Active Ingredient Unit: mg/1
Pharm Classes: Norepinephrine Uptake Inhibitors [MoA],Serotonin and Norepinephrine Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]
DEA Schedule: