Package 16714-067-01

Brand: carbidopa

Generic: carbidopa
NDC Package

Package Facts

Identity

Package NDC 16714-067-01
Digits Only 1671406701
Product NDC 16714-067
Product ID 16714-067_65000b5a-3d2e-4228-8757-cca85e663c80
Description

100 TABLET in 1 BOTTLE (16714-067-01)

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": "65000b5a-3d2e-4228-8757-cca85e663c80", "openfda": {"nui": ["N0000175754", "N0000175755"], "unii": ["MNX7R8C5VO"], "rxcui": ["260260"], "spl_set_id": ["33ee4598-cbcc-45e0-a48e-dc0101e1f204"], "pharm_class_epc": ["Aromatic Amino Acid Decarboxylation Inhibitor [EPC]"], "pharm_class_moa": ["DOPA Decarboxylase Inhibitors [MoA]"], "manufacturer_name": ["NorthStar Rx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (16714-067-01)", "package_ndc": "16714-067-01", "marketing_start_date": "20191021"}], "brand_name": "Carbidopa", "product_id": "16714-067_65000b5a-3d2e-4228-8757-cca85e663c80", "dosage_form": "TABLET", "product_ndc": "16714-067", "generic_name": "Carbidopa", "labeler_name": "NorthStar Rx LLC", "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"}