Package 0069-0501-30
Brand: xeljanz xr
Generic: tofacitinibPackage Facts
Identity
Package NDC
0069-0501-30
Digits Only
0069050130
Product NDC
0069-0501
Description
30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0069-0501-30)
Marketing
Marketing Status
Brand
xeljanz xr
Generic
tofacitinib
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "60d5a945-0cec-4730-854b-d675fc116621", "openfda": {"upc": ["0300691002018", "0300691001011"], "unii": ["O1FF4DIV0D"], "rxcui": ["1357541", "1357547", "1741046", "1741049", "2048566", "2048568", "2273113", "2273115", "2478433", "2478437"], "spl_set_id": ["cf74ba2f-afc5-4baa-8594-979c889a5831"], "manufacturer_name": ["Pfizer Laboratories Div Pfizer Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0069-0501-30)", "package_ndc": "0069-0501-30", "marketing_start_date": "20160307"}], "brand_name": "XELJANZ XR", "product_id": "0069-0501_60d5a945-0cec-4730-854b-d675fc116621", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Janus Kinase Inhibitor [EPC]", "Janus Kinase Inhibitors [MoA]"], "product_ndc": "0069-0501", "generic_name": "tofacitinib", "labeler_name": "Pfizer Laboratories Div Pfizer Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "XELJANZ", "brand_name_suffix": "XR", "active_ingredients": [{"name": "TOFACITINIB CITRATE", "strength": "11 mg/1"}], "application_number": "NDA208246", "marketing_category": "NDA", "marketing_start_date": "20160307", "listing_expiration_date": "20271231"}