Package 68071-3767-6

Brand: mycophenolate mofetil

Generic: mycophenolate mofetil
NDC Package

Package Facts

Identity

Package NDC 68071-3767-6
Digits Only 6807137676
Product NDC 68071-3767
Product ID 68071-3767_2b9b049f-8ec4-0535-e063-6394a90afc7a
Description

60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68071-3767-6)

Marketing

Marketing Status
Marketed Since 2025-01-13
Brand mycophenolate mofetil
Generic mycophenolate mofetil
Sample Package No

Linked Drug Pages (1)

Mycophenolate mofetil ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2b9b049f-8ec4-0535-e063-6394a90afc7a", "openfda": {"upc": ["0368071376760"], "unii": ["9242ECW6R0"], "rxcui": ["200060"], "spl_set_id": ["2b9ae8ff-f2bc-ccef-e063-6294a90a76da"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68071-3767-6)", "package_ndc": "68071-3767-6", "marketing_start_date": "20250113"}], "brand_name": "Mycophenolate mofetil", "product_id": "68071-3767_2b9b049f-8ec4-0535-e063-6394a90afc7a", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antimetabolite Immunosuppressant [EPC]"], "product_ndc": "68071-3767", "generic_name": "Mycophenolate mofetil", "labeler_name": "NuCare Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Mycophenolate mofetil", "active_ingredients": [{"name": "MYCOPHENOLATE MOFETIL", "strength": "500 mg/1"}], "application_number": "ANDA090456", "marketing_category": "ANDA", "marketing_start_date": "20101106", "listing_expiration_date": "20261231"}