Package 70710-1221-1

Brand: carbidopa

Generic: carbidopa
NDC Package

Package Facts

Identity

Package NDC 70710-1221-1
Digits Only 7071012211
Product NDC 70710-1221
Product ID 70710-1221_3abe5c9f-1e44-4fe7-b5d1-70f66f2bcfe1
Description

100 TABLET in 1 BOTTLE (70710-1221-1)

Marketing

Marketing Status
Marketed Since 2018-09-06
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": "3abe5c9f-1e44-4fe7-b5d1-70f66f2bcfe1", "openfda": {"nui": ["N0000175754", "N0000175755"], "unii": ["MNX7R8C5VO"], "rxcui": ["260260"], "spl_set_id": ["c0b1ef99-3092-431a-8fb6-897affd52595"], "pharm_class_epc": ["Aromatic Amino Acid Decarboxylation Inhibitor [EPC]"], "pharm_class_moa": ["DOPA Decarboxylase Inhibitors [MoA]"], "manufacturer_name": ["Zydus Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (70710-1221-1)", "package_ndc": "70710-1221-1", "marketing_start_date": "20180906"}], "brand_name": "CARBIDOPA", "product_id": "70710-1221_3abe5c9f-1e44-4fe7-b5d1-70f66f2bcfe1", "dosage_form": "TABLET", "product_ndc": "70710-1221", "generic_name": "CARBIDOPA", "labeler_name": "Zydus Pharmaceuticals USA Inc.", "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"}