Package 42799-123-01

Brand: carbidopa

Generic: carbidopa
NDC Package

Package Facts

Identity

Package NDC 42799-123-01
Digits Only 4279912301
Product NDC 42799-123
Description

100 TABLET in 1 BOTTLE (42799-123-01)

Marketing

Marketing Status
Marketed Since 2016-02-19
Brand carbidopa
Generic carbidopa
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "462dd421-0006-e25d-e063-6294a90ad0ef", "openfda": {"nui": ["N0000175754", "N0000175755"], "upc": ["0342799123011"], "unii": ["MNX7R8C5VO"], "rxcui": ["260260"], "spl_set_id": ["55b99f22-9eb2-4df6-9979-bc4c3af5e454"], "pharm_class_epc": ["Aromatic Amino Acid Decarboxylation Inhibitor [EPC]"], "pharm_class_moa": ["DOPA Decarboxylase Inhibitors [MoA]"], "manufacturer_name": ["Edenbridge Pharmaceuticals LLC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (42799-123-01)", "package_ndc": "42799-123-01", "marketing_start_date": "20160219"}], "brand_name": "Carbidopa", "product_id": "42799-123_462dd421-0006-e25d-e063-6294a90ad0ef", "dosage_form": "TABLET", "product_ndc": "42799-123", "generic_name": "Carbidopa", "labeler_name": "Edenbridge Pharmaceuticals LLC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Carbidopa", "active_ingredients": [{"name": "CARBIDOPA", "strength": "25 mg/1"}], "application_number": "ANDA205304", "marketing_category": "ANDA", "marketing_start_date": "20160219", "listing_expiration_date": "20261231"}