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ATOMOXETINE

NDC 82619-121 · HUMAN PRESCRIPTION DRUG · CAPSULE

Generic nameatomoxetine
Labeler / ManufacturerCreekwood Pharmaceuticals LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA218875
Dosage form / routeCAPSULE · ORAL
Active ingredientsATOMOXETINE HYDROCHLORIDE (100 mg/1)
Marketing started20260706
Package count2

External sources

Source: openFDA. Public-domain (CC0).