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Duloxetine

NDC 25000-608 · HUMAN PRESCRIPTION DRUG · CAPSULE, DELAYED RELEASE

Generic nameDuloxetine Hydrochloride
Labeler / ManufacturerMARKSANS PHARMA LIMITED
Marketing categoryAbbreviated NDA (generic) · App ANDA090723
Dosage form / routeCAPSULE, DELAYED RELEASE · ORAL
Active ingredientsDULOXETINE HYDROCHLORIDE (20 mg/1)
Marketing started20220527
Package count1

External sources

Source: openFDA. Public-domain (CC0).