FDA NDC Directory · JSON-LD · Markdown

Tolmetin Sodium

NDC 16571-826 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerRising Pharma Holdings, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA073393
Dosage form / routeCAPSULE · ORAL
Active ingredientsTOLMETIN SODIUM (400 mg/1)
Marketing started20230630
Marketing ended20260531
Package count1

External sources

Source: openFDA. Public-domain (CC0).