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Nortriptyline Hydrochloride

NDC 76420-913 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerAsclemed USA, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA073556
Dosage form / routeCAPSULE · ORAL
Active ingredientsNORTRIPTYLINE HYDROCHLORIDE (75 mg/1)
Marketing started20231117
Package count4

External sources

Source: openFDA. Public-domain (CC0).