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"70095-008-02" National Drug Code (NDC)
Tofacitinib 1 BOTTLE in 1 CARTON (70095-008-02) / 240 mL in 1 BOTTLE
(Sun Pharmaceutical Industries, Inc.)
NDC Code
70095-008-02
Package Description
1 BOTTLE in 1 CARTON (70095-008-02) / 240 mL in 1 BOTTLE
Product NDC
70095-008
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Tofacitinib
Non-Proprietary Name
Tofacitinib
Dosage Form
SOLUTION
Usage
ORAL
Start Marketing Date
20260603
Marketing Category Name
ANDA
Application Number
ANDA218407
Manufacturer
Sun Pharmaceutical Industries, Inc.
Substance Name
TOFACITINIB CITRATE
Strength
1
Strength Unit
mg/mL
Pharmacy Classes
Janus Kinase Inhibitor [EPC], Janus Kinase Inhibitors [MoA]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/70095-008-02