xeljanz
Generic: tofacitinib
Labeler: u.s. pharmaceuticalsDrug Facts
Product Profile
Brand Name
xeljanz
Generic Name
tofacitinib
Labeler
u.s. pharmaceuticals
Dosage Form
SOLUTION
Routes
Active Ingredients
tofacitinib citrate 1 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
63539-029
Product ID
63539-029_c422393a-1e5c-46d2-81df-3d05818bf50e
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA
Application Number
NDA213082
Listing Expiration
2027-12-31
Marketing Start
2021-02-08
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
63539029
Hyphenated Format
63539-029
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
xeljanz (source: ndc)
Generic Name
tofacitinib (source: ndc)
Application Number
NDA213082 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1 mg/mL
Packaging
- 1 BOTTLE in 1 CARTON (63539-029-02) / 240 mL in 1 BOTTLE (63539-029-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "c422393a-1e5c-46d2-81df-3d05818bf50e", "openfda": {"unii": ["O1FF4DIV0D"], "rxcui": ["1357541", "1357547", "1741046", "1741049", "2048566", "2048568", "2273113", "2273115", "2478433", "2478437"], "spl_set_id": ["68e3d6b2-7838-4d2d-a417-09d919b43e13"], "manufacturer_name": ["U.S. Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (63539-029-02) / 240 mL in 1 BOTTLE (63539-029-01)", "package_ndc": "63539-029-02", "marketing_start_date": "20210208"}], "brand_name": "XELJANZ", "product_id": "63539-029_c422393a-1e5c-46d2-81df-3d05818bf50e", "dosage_form": "SOLUTION", "pharm_class": ["Janus Kinase Inhibitor [EPC]", "Janus Kinase Inhibitors [MoA]"], "product_ndc": "63539-029", "generic_name": "tofacitinib", "labeler_name": "U.S. Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "XELJANZ", "active_ingredients": [{"name": "TOFACITINIB CITRATE", "strength": "1 mg/mL"}], "application_number": "NDA213082", "marketing_category": "NDA", "marketing_start_date": "20210208", "listing_expiration_date": "20271231"}