"70801-003-01" National Drug Code (NDC)

Zilretta 1 KIT in 1 CARTON (70801-003-01) * 1 INJECTION, POWDER, FOR SUSPENSION, EXTENDED RELEASE in 1 VIAL, SINGLE-DOSE (70801-001-02) * 1 INJECTION, SOLUTION in 1 VIAL, SINGLE-DOSE (70801-002-02) * 1 INJECTION, POWDER, FOR SUSPENSION, EXTENDED RELEASE in 1 VIAL, SINGLE-DOSE (70801-001-01) * 1 INJECTION, SOLUTION in 1 VIAL, SINGLE-DOSE (70801-002-01)
(Flexion Therapeutics, Inc.)

NDC Code70801-003-01
Package Description1 KIT in 1 CARTON (70801-003-01) * 1 INJECTION, POWDER, FOR SUSPENSION, EXTENDED RELEASE in 1 VIAL, SINGLE-DOSE (70801-001-02) * 1 INJECTION, SOLUTION in 1 VIAL, SINGLE-DOSE (70801-002-02) * 1 INJECTION, POWDER, FOR SUSPENSION, EXTENDED RELEASE in 1 VIAL, SINGLE-DOSE (70801-001-01) * 1 INJECTION, SOLUTION in 1 VIAL, SINGLE-DOSE (70801-002-01)
Product NDC70801-003
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameZilretta
Non-Proprietary NameTriamcinolone Acetonide Extended-release Injectable Suspension
Dosage FormKIT
UsageINTRA-ARTICULAR
Start Marketing Date20171006
End Marketing Date20230331
Marketing Category NameNDA
Application NumberNDA208845
ManufacturerFlexion Therapeutics, Inc.

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