FDA NDC Directory · JSON-LD · Markdown

Meclofenamate Sodium

NDC 0378-2150 · HUMAN PRESCRIPTION DRUG · CAPSULE

Generic namemeclofenamate sodium
Labeler / ManufacturerMylan Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA071081
Dosage form / routeCAPSULE · ORAL
Active ingredientsMECLOFENAMATE SODIUM (50 mg/1)
Marketing started19860903
Package count1

External sources

Source: openFDA. Public-domain (CC0).