FDA NDC Directory · JSON-LD · Markdown

Betaine

NDC 0713-0352 · HUMAN PRESCRIPTION DRUG · POWDER, FOR SOLUTION

Labeler / ManufacturerCosette Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA214864
Dosage form / routePOWDER, FOR SOLUTION · ORAL
Active ingredientsBETAINE (1 g/g)
Marketing started20230101
Package count1

External sources

Source: openFDA. Public-domain (CC0).