FDA NDC Directory · JSON-LD · Markdown

Isosorbide Mononitrate

NDC 42677-307 · HUMAN PRESCRIPTION DRUG · TABLET, EXTENDED RELEASE

Labeler / ManufacturerShandong New Time Pharmaceutical Co., Ltd.
Marketing categoryAbbreviated NDA (generic) · App ANDA214115
Dosage form / routeTABLET, EXTENDED RELEASE · ORAL
Active ingredientsISOSORBIDE MONONITRATE (120 mg/1)
Marketing started20220429
Package count2

External sources

Source: openFDA. Public-domain (CC0).