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Atomoxetine Hydrochloride - Atomoxetine Hydrochloride

Navigation: NDC > Supplier starting with: S > SUN PHARMA GLOBAL FZE
Field Value
NDC Code: 47335-820
Proprietary Name: Atomoxetine Hydrochloride
Suffix:
Non-Proprietary Name: Atomoxetine Hydrochloride
Dosage Form: CAPSULE
Method: ORAL
Original Marketing Date: 05-10-2010
Category Name: ANDA
Application Number: ANDA079020
Labeler: SUN PHARMA GLOBAL FZE
Substance Name: ATOMOXETINE HYDROCHLORIDE
Active Numerator Strength: 100
Active Ingredient Unit: mg/1
Pharm Classes: Norepinephrine Reuptake Inhibitor [EPC],Norepinephrine Uptake Inhibitors [MoA]
DEA Schedule: