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Atomoxetine Hydrochloride

NDC 70518-4313 · HUMAN PRESCRIPTION DRUG · CAPSULE

Generic nameatomoxetine hydrochloride
Labeler / ManufacturerREMEDYREPACK INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA078983
Dosage form / routeCAPSULE · ORAL
Active ingredientsATOMOXETINE HYDROCHLORIDE (10 mg/1)
Marketing started20250319
Package count1

External sources

Source: openFDA. Public-domain (CC0).