Package 62756-457-88
Brand: carbidopa and levodopa
Generic: carbidopa and levodopaPackage Facts
Identity
Package NDC
62756-457-88
Digits Only
6275645788
Product NDC
62756-457
Description
100 TABLET, EXTENDED RELEASE in 1 BOTTLE (62756-457-88)
Marketing
Marketing Status
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": "91ce9c25-03a0-40d1-a463-60929a93114e", "openfda": {"nui": ["N0000193220", "M0370111", "N0000175754", "N0000175755"], "upc": ["0362756457836"], "unii": ["46627O600J", "MNX7R8C5VO"], "rxcui": ["308988", "308989"], "spl_set_id": ["d2a64f14-f638-49d9-8a96-cb7ae46ac3ea"], "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, EXTENDED RELEASE in 1 BOTTLE (62756-457-08)", "package_ndc": "62756-457-08", "marketing_start_date": "20070823"}, {"sample": false, "description": "1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (62756-457-18)", "package_ndc": "62756-457-18", "marketing_start_date": "20070823"}, {"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (62756-457-83)", "package_ndc": "62756-457-83", "marketing_start_date": "20070823"}, {"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (62756-457-88)", "package_ndc": "62756-457-88", "marketing_start_date": "20070823"}], "brand_name": "CARBIDOPA AND LEVODOPA", "product_id": "62756-457_91ce9c25-03a0-40d1-a463-60929a93114e", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Amino Acids", "Aromatic [CS]", "Aromatic Amino Acid [EPC]"], "product_ndc": "62756-457", "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": "50 mg/1"}, {"name": "LEVODOPA", "strength": "200 mg/1"}], "application_number": "ANDA077828", "marketing_category": "ANDA", "marketing_start_date": "20070823", "listing_expiration_date": "20261231"}