Package 62756-517-08

Brand: carbidopa and levodopa

Generic: carbidopa and levodopa
NDC Package

Package Facts

Identity

Package NDC 62756-517-08
Digits Only 6275651708
Product NDC 62756-517
Description

100 TABLET in 1 BOTTLE (62756-517-08)

Marketing

Marketing Status
Marketed Since 2008-10-28
Brand carbidopa and levodopa
Generic carbidopa and levodopa
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "d77ed25a-588d-4d22-855f-f93ba5b4003c", "openfda": {"nui": ["N0000193220", "M0370111", "N0000175754", "N0000175755"], "upc": ["0362756517882", "0362756519886", "0362756518889"], "unii": ["46627O600J", "MNX7R8C5VO"], "rxcui": ["197443", "197444", "197445"], "spl_set_id": ["829c35f9-ace0-11dd-8800-f3e252b43544"], "pharm_class_cs": ["Amino Acids, Aromatic [CS]"], "pharm_class_epc": ["Aromatic Amino Acid [EPC]", "Aromatic Amino Acid Decarboxylation Inhibitor [EPC]"], "pharm_class_moa": ["DOPA Decarboxylase Inhibitors [MoA]"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (62756-517-08)", "package_ndc": "62756-517-08", "marketing_start_date": "20081028"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (62756-517-13)", "package_ndc": "62756-517-13", "marketing_start_date": "20081028"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (62756-517-18)", "package_ndc": "62756-517-18", "marketing_start_date": "20081028"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (62756-517-83)", "package_ndc": "62756-517-83", "marketing_start_date": "20081028"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (62756-517-88)", "package_ndc": "62756-517-88", "marketing_start_date": "20081028"}], "brand_name": "CARBIDOPA AND LEVODOPA", "product_id": "62756-517_d77ed25a-588d-4d22-855f-f93ba5b4003c", "dosage_form": "TABLET", "pharm_class": ["Amino Acids", "Aromatic [CS]", "Aromatic Amino Acid [EPC]"], "product_ndc": "62756-517", "generic_name": "CARBIDOPA AND LEVODOPA", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CARBIDOPA AND LEVODOPA", "active_ingredients": [{"name": "CARBIDOPA", "strength": "10 mg/1"}, {"name": "LEVODOPA", "strength": "100 mg/1"}], "application_number": "ANDA078536", "marketing_category": "ANDA", "marketing_start_date": "20081028", "listing_expiration_date": "20261231"}