Package 68071-1749-1

Brand: sucralfate

Generic: sucralfate
NDC Package

Package Facts

Identity

Package NDC 68071-1749-1
Digits Only 6807117491
Product NDC 68071-1749
Product ID 68071-1749_1d511cb3-fe46-576f-e063-6394a90a2b9f
Description

100 TABLET in 1 BOTTLE (68071-1749-1)

Marketing

Marketing Status
Marketed Since 2020-04-24
Brand sucralfate
Generic sucralfate
Sample Package No

Linked Drug Pages (1)

Sucralfate ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "1d511cb3-fe46-576f-e063-6394a90a2b9f", "openfda": {"nui": ["N0000175801", "M0015420"], "upc": ["0368071174915"], "unii": ["XX73205DH5"], "rxcui": ["314234"], "spl_set_id": ["a40e43d4-9240-34ad-e053-2995a90a98e1"], "pharm_class_cs": ["Organometallic Compounds [CS]"], "pharm_class_epc": ["Aluminum Complex [EPC]"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (68071-1749-1)", "package_ndc": "68071-1749-1", "marketing_start_date": "20200424"}], "brand_name": "Sucralfate", "product_id": "68071-1749_1d511cb3-fe46-576f-e063-6394a90a2b9f", "dosage_form": "TABLET", "pharm_class": ["Aluminum Complex [EPC]", "Organometallic Compounds [CS]"], "product_ndc": "68071-1749", "generic_name": "Sucralfate", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sucralfate", "active_ingredients": [{"name": "SUCRALFATE", "strength": "1 g/1"}], "application_number": "ANDA070848", "marketing_category": "ANDA", "marketing_start_date": "19961111", "listing_expiration_date": "20261231"}