FDA Orange Book · active-ingredient family
Sodium chromate cr-51
Sodium chromate cr-51 is approved in 2 FDA applications, with therapeutic-equivalence codes, listed patents, and marketing exclusivity from the FDA Orange Book.
Reference-listed drug:CHROMITOPE SODIUM · NDA 013993
2
Brand (NDA)
0
Generics (ANDA)
0
Listed patents
0
Exclusivity periods
Brand (NDA) products · injectable
| Product | Applicant | Application | TE | Approved | |
|---|---|---|---|---|---|
| CHROMITOPE SODIUM×2 | BRACCO | NDA 013993 | — | Approved Prior to Jan 1, 1982 | |
| SODIUM CHROMATE CR 51 | CURIUM | NDA 016708 | — | Approved Prior to Jan 1, 1982 |
Listed patents
No patents are listed against this product in the Orange Book. Listed patents reflect those the NDA holder submits under 21 U.S.C. 355 and are not exhaustive.
Sodium chromate cr-51 — frequently asked questions
Generics, reference-listed drug, patents, and exclusivity for this active ingredient, from the FDA Orange Book.

