← FDA Drug Approvals (Drugs@FDA)

CHROMITOPE SODIUM

NDA · New Drug Application · Sponsor: BRACCO · Approved 1971-12-27

Drug application

FDA Application #

NDA013993

Application type

New Drug Application

Brand name

CHROMITOPE SODIUM

Generic name

Sodium Chromate Cr-51

Active ingredients

SODIUM CHROMATE CR-51

Dosage form

INJECTABLE

Route

INJECTION

Marketing status

Discontinued

Sponsor

BRACCO

First approval

1971-12-27

Source

Authoritative

Drugs@FDA application overview

Machine

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