Package 70771-1355-1

Brand: carbidopa

Generic: carbidopa
NDC Package

Package Facts

Identity

Package NDC 70771-1355-1
Digits Only 7077113551
Product NDC 70771-1355
Description

100 TABLET in 1 BOTTLE (70771-1355-1)

Marketing

Marketing Status
Marketed Since 2018-09-06
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": "46adf313-2cc6-42be-ab34-627223b59ad6", "openfda": {"nui": ["N0000175754", "N0000175755"], "upc": ["0370710122119"], "unii": ["MNX7R8C5VO"], "rxcui": ["260260"], "spl_set_id": ["83012ccc-aba2-45bb-9326-dc30cdeb4e3b"], "pharm_class_epc": ["Aromatic Amino Acid Decarboxylation Inhibitor [EPC]"], "pharm_class_moa": ["DOPA Decarboxylase Inhibitors [MoA]"], "manufacturer_name": ["Zydus Lifesciences Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (70771-1355-1)", "package_ndc": "70771-1355-1", "marketing_start_date": "20180906"}], "brand_name": "CARBIDOPA", "product_id": "70771-1355_46adf313-2cc6-42be-ab34-627223b59ad6", "dosage_form": "TABLET", "product_ndc": "70771-1355", "generic_name": "CARBIDOPA", "labeler_name": "Zydus Lifesciences Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CARBIDOPA", "active_ingredients": [{"name": "CARBIDOPA", "strength": "25 mg/1"}], "application_number": "ANDA209910", "marketing_category": "ANDA", "marketing_start_date": "20180906", "listing_expiration_date": "20261231"}