Package 31722-889-30

Brand: fingolimod

Generic: fingolimod
NDC Package

Package Facts

Identity

Package NDC 31722-889-30
Digits Only 3172288930
Product NDC 31722-889
Product ID 31722-889_46342e58-9ad6-7e95-e063-6294a90aa7b4
Description

30 CAPSULE in 1 BOTTLE (31722-889-30)

Marketing

Marketing Status
Marketed Since 2019-09-27
Brand fingolimod
Generic fingolimod
Sample Package No

Linked Drug Pages (1)

Fingolimod ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "46342e58-9ad6-7e95-e063-6294a90aa7b4", "openfda": {"upc": ["0331722889308"], "unii": ["G926EC510T"], "rxcui": ["1012895"], "spl_set_id": ["c3199508-3d6a-4e44-96f0-bbde9969edcb"], "manufacturer_name": ["Camber Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE (31722-889-30)", "package_ndc": "31722-889-30", "marketing_start_date": "20190927"}], "brand_name": "Fingolimod", "product_id": "31722-889_46342e58-9ad6-7e95-e063-6294a90aa7b4", "dosage_form": "CAPSULE", "pharm_class": ["Sphingosine 1-Phosphate Receptor Modulators [MoA]", "Sphingosine 1-phosphate Receptor Modulator [EPC]"], "product_ndc": "31722-889", "generic_name": "Fingolimod", "labeler_name": "Camber Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fingolimod", "active_ingredients": [{"name": "FINGOLIMOD HYDROCHLORIDE", "strength": ".5 mg/1"}], "application_number": "ANDA207933", "marketing_category": "ANDA", "marketing_start_date": "20190927", "listing_expiration_date": "20261231"}