FDA NDC Directory · JSON-LD · Markdown

Calcium Acetate

NDC 69097-862 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerCipla USA Inc.,
Marketing categoryAbbreviated NDA (generic) · App ANDA203135
Dosage form / routeCAPSULE · ORAL
Active ingredientsCALCIUM ACETATE (667 mg/1)
Marketing started20160726
Package count2

External sources

Source: openFDA. Public-domain (CC0).