FDA NDC Directory · JSON-LD · Markdown

HYDROXYCHLOROQUINE SULFATE

NDC 43598-133 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerDr. Reddy's Laboratories Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA210441
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsHYDROXYCHLOROQUINE SULFATE (100 mg/1)
Marketing started20221024
Package count2

External sources

Source: openFDA. Public-domain (CC0).