Package 0781-2102-01

Brand: tacrolimus

Generic: tacrolimus
NDC Package

Package Facts

Identity

Package NDC 0781-2102-01
Digits Only 0781210201
Product NDC 0781-2102
Product ID 0781-2102_8f214e2d-762b-4a1b-bf23-0f784d91a8c2
Description

100 CAPSULE in 1 BOTTLE (0781-2102-01)

Marketing

Marketing Status
Marketed Since 2009-08-10
Brand tacrolimus
Generic tacrolimus
Sample Package No

Linked Drug Pages (1)

Tacrolimus ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "8f214e2d-762b-4a1b-bf23-0f784d91a8c2", "openfda": {"upc": ["0307812103012", "0307812102015", "0307812104019"], "unii": ["WM0HAQ4WNM"], "rxcui": ["198377", "198378", "313190"], "spl_set_id": ["46ac55cf-d85e-4c34-bb33-f49e078c4a03"], "manufacturer_name": ["Sandoz Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (0781-2102-01)", "package_ndc": "0781-2102-01", "marketing_start_date": "20090810"}], "brand_name": "Tacrolimus", "product_id": "0781-2102_8f214e2d-762b-4a1b-bf23-0f784d91a8c2", "dosage_form": "CAPSULE", "pharm_class": ["Calcineurin Inhibitor Immunosuppressant [EPC]", "Calcineurin Inhibitors [MoA]"], "product_ndc": "0781-2102", "generic_name": "Tacrolimus", "labeler_name": "Sandoz Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tacrolimus", "active_ingredients": [{"name": "TACROLIMUS", "strength": ".5 mg/1"}], "application_number": "ANDA065461", "marketing_category": "ANDA", "marketing_start_date": "20090810", "listing_expiration_date": "20261231"}