FDA NDC Directory · JSON-LD · Markdown

Duloxetine

NDC 55700-605 · HUMAN PRESCRIPTION DRUG · CAPSULE, DELAYED RELEASE

Labeler / ManufacturerQuality Care Products LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA208706
Dosage form / routeCAPSULE, DELAYED RELEASE · ORAL
Active ingredientsDULOXETINE HYDROCHLORIDE (30 mg/1)
Marketing started20180420
Marketing ended20260531
Package count2

External sources

Source: openFDA. Public-domain (CC0).