Package 47335-188-88

Brand: carbidopa and levodopa

Generic: carbidopa and levodopa
NDC Package

Package Facts

Identity

Package NDC 47335-188-88
Digits Only 4733518888
Product NDC 47335-188
Description

100 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (47335-188-88)

Marketing

Marketing Status
Marketed Since 2014-12-15
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": "5c297458-6e97-4222-8a82-1b28928ce796", "openfda": {"nui": ["N0000193220", "M0370111", "N0000175754", "N0000175755"], "unii": ["46627O600J", "MNX7R8C5VO"], "rxcui": ["476399", "476515", "483090"], "spl_set_id": ["48e0f2ec-b217-4c25-a71c-20e173d05edb"], "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, ORALLY DISINTEGRATING in 1 BOTTLE (47335-188-08)", "package_ndc": "47335-188-08", "marketing_start_date": "20141215"}, {"sample": false, "description": "1000 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (47335-188-18)", "package_ndc": "47335-188-18", "marketing_start_date": "20141215"}, {"sample": false, "description": "30 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (47335-188-83)", "package_ndc": "47335-188-83", "marketing_start_date": "20141215"}, {"sample": false, "description": "100 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (47335-188-88)", "package_ndc": "47335-188-88", "marketing_start_date": "20141215"}], "brand_name": "CARBIDOPA AND LEVODOPA", "product_id": "47335-188_5c297458-6e97-4222-8a82-1b28928ce796", "dosage_form": "TABLET, ORALLY DISINTEGRATING", "pharm_class": ["Amino Acids", "Aromatic [CS]", "Aromatic Amino Acid [EPC]"], "product_ndc": "47335-188", "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": "25 mg/1"}, {"name": "LEVODOPA", "strength": "250 mg/1"}], "application_number": "ANDA078690", "marketing_category": "ANDA", "marketing_start_date": "20141215", "listing_expiration_date": "20261231"}