Package 68682-200-25

Brand: carbidopa

Generic: carbidopa tablets
NDC Package

Package Facts

Identity

Package NDC 68682-200-25
Digits Only 6868220025
Product NDC 68682-200
Product ID 68682-200_ccf10efe-4fda-40a4-8f20-1ccefb151a15
Description

100 TABLET in 1 BOTTLE (68682-200-25)

Marketing

Marketing Status
Marketed Since 2014-04-04
Brand carbidopa
Generic carbidopa tablets
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": "ccf10efe-4fda-40a4-8f20-1ccefb151a15", "openfda": {"nui": ["N0000175754", "N0000175755"], "unii": ["MNX7R8C5VO"], "rxcui": ["260260"], "spl_set_id": ["d5204e5e-10ef-4758-8fc6-cb710048c687"], "pharm_class_epc": ["Aromatic Amino Acid Decarboxylation Inhibitor [EPC]"], "pharm_class_moa": ["DOPA Decarboxylase Inhibitors [MoA]"], "manufacturer_name": ["Oceanside Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (68682-200-25)", "package_ndc": "68682-200-25", "marketing_start_date": "20140404"}], "brand_name": "Carbidopa", "product_id": "68682-200_ccf10efe-4fda-40a4-8f20-1ccefb151a15", "dosage_form": "TABLET", "product_ndc": "68682-200", "generic_name": "Carbidopa Tablets", "labeler_name": "Oceanside Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Carbidopa", "active_ingredients": [{"name": "CARBIDOPA", "strength": "25 mg/1"}], "application_number": "NDA017830", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20140404", "listing_expiration_date": "20261231"}