Package 59651-146-01

Brand: carbidopa

Generic: carbidopa
NDC Package

Package Facts

Identity

Package NDC 59651-146-01
Digits Only 5965114601
Product NDC 59651-146
Product ID 59651-146_b5de1a51-8312-467a-9522-2e6a4046266d
Description

100 TABLET in 1 BOTTLE (59651-146-01)

Marketing

Marketing Status
Marketed Since 2019-10-21
Brand carbidopa
Generic carbidopa
Sample Package No

Linked Drug Pages (1)

Carbidopa ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "b5de1a51-8312-467a-9522-2e6a4046266d", "openfda": {"nui": ["N0000175754", "N0000175755"], "unii": ["MNX7R8C5VO"], "rxcui": ["260260"], "spl_set_id": ["ed98c7e1-78a6-43a5-92cd-4f085af6f09d"], "pharm_class_epc": ["Aromatic Amino Acid Decarboxylation Inhibitor [EPC]"], "pharm_class_moa": ["DOPA Decarboxylase Inhibitors [MoA]"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (59651-146-01)", "package_ndc": "59651-146-01", "marketing_start_date": "20191021"}], "brand_name": "Carbidopa", "product_id": "59651-146_b5de1a51-8312-467a-9522-2e6a4046266d", "dosage_form": "TABLET", "product_ndc": "59651-146", "generic_name": "Carbidopa", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Carbidopa", "active_ingredients": [{"name": "CARBIDOPA", "strength": "25 mg/1"}], "application_number": "ANDA211055", "marketing_category": "ANDA", "marketing_start_date": "20191021", "listing_expiration_date": "20261231"}