FDA Orange Book · active-ingredient family
Tubocurarine chloride
Tubocurarine chloride is approved in 3 FDA applications, with therapeutic-equivalence codes, listed patents, and marketing exclusivity from the FDA Orange Book.
Reference-listed drug:TUBOCURARINE CHLORIDE · NDA 005657
3
Brand (NDA)
0
Generics (ANDA)
0
Listed patents
0
Exclusivity periods
Brand (NDA) products · injectable
| Product | Applicant | Application | TE | Approved | |
|---|---|---|---|---|---|
| TUBOCURARINE CHLORIDE | BRISTOL MYERS SQUIBB | NDA 005657 | — | Approved Prior to Jan 1, 1982 | |
| TUBOCURARINE CHLORIDE | HOSPIRA | NDA 006095 | — | Approved Prior to Jan 1, 1982 | |
| TUBOCURARINE CHLORIDE | LILLY | NDA 006325 | — | 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.
Tubocurarine chloride — frequently asked questions
Generics, reference-listed drug, patents, and exclusivity for this active ingredient, from the FDA Orange Book.

