Package 70771-1833-1

Brand: sucralfate

Generic: sucralfate
NDC Package

Package Facts

Identity

Package NDC 70771-1833-1
Digits Only 7077118331
Product NDC 70771-1833
Description

100 TABLET in 1 BOTTLE (70771-1833-1)

Marketing

Marketing Status
Marketed Since 2023-05-20
Brand sucralfate
Generic sucralfate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "f0b6479d-234b-426c-8035-6e4675d8853a", "openfda": {"nui": ["N0000175801", "M0015420"], "unii": ["XX73205DH5"], "rxcui": ["314234"], "spl_set_id": ["882b7596-f62c-4be2-8f67-e64310718baa"], "pharm_class_cs": ["Organometallic Compounds [CS]"], "pharm_class_epc": ["Aluminum Complex [EPC]"], "manufacturer_name": ["Zydus Lifesciences Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (70771-1833-1)", "package_ndc": "70771-1833-1", "marketing_start_date": "20230520"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (70771-1833-3)", "package_ndc": "70771-1833-3", "marketing_start_date": "20230520"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (70771-1833-5)", "package_ndc": "70771-1833-5", "marketing_start_date": "20230520"}], "brand_name": "Sucralfate", "product_id": "70771-1833_f0b6479d-234b-426c-8035-6e4675d8853a", "dosage_form": "TABLET", "pharm_class": ["Aluminum Complex [EPC]", "Organometallic Compounds [CS]"], "product_ndc": "70771-1833", "generic_name": "Sucralfate", "labeler_name": "Zydus Lifesciences Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sucralfate", "active_ingredients": [{"name": "SUCRALFATE", "strength": "1 g/1"}], "application_number": "ANDA215705", "marketing_category": "ANDA", "marketing_start_date": "20230520", "listing_expiration_date": "20261231"}