FDA NDC Directory · JSON-LD · Markdown

Loperamide Hydrochloride

NDC 42799-605 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerEdenbridge Pharmaceuticals LLC.
Marketing categoryAbbreviated NDA (generic) · App ANDA215001
Dosage form / routeCAPSULE · ORAL
Active ingredientsLOPERAMIDE HYDROCHLORIDE (2 mg/1)
Marketing started20200925
Package count3

External sources

Source: openFDA. Public-domain (CC0).