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Doxepin Hydrochloride

NDC 24658-797 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerPURACAP LABORATORIES LLC DBA BLU PHARMACEUTICALS
Marketing categoryAbbreviated NDA (generic) · App ANDA210675
Dosage form / routeCAPSULE · ORAL
Active ingredientsDOXEPIN HYDROCHLORIDE (100 mg/1)
Marketing started20230314
Package count3

External sources

Source: openFDA. Public-domain (CC0).