Package 68001-172-00

Brand: CARBIDOPA AND LEVODOPA

Generic: Carbidopa and Levodopa
NDC Package

Package Facts

Identity

Package NDC 68001-172-00
Digits Only 6800117200
Product NDC 68001-172
Description

100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68001-172-00)

Marketing

Marketing Status
Discontinued 2026-02-28
Brand CARBIDOPA AND LEVODOPA
Generic Carbidopa and Levodopa
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "304c30d1-a315-0451-e063-6294a90abb9f", "openfda": {"nui": ["N0000193220", "M0370111", "N0000175754", "N0000175755"], "upc": ["0368001172004", "0368001171007"], "unii": ["46627O600J", "MNX7R8C5VO"], "rxcui": ["308988", "308989"], "spl_set_id": ["58a6e76a-f99f-4f0c-9d83-a55a30edda97"], "pharm_class_cs": ["Amino Acids, Aromatic [CS]"], "pharm_class_epc": ["Aromatic Amino Acid [EPC]", "Aromatic Amino Acid Decarboxylation Inhibitor [EPC]"], "pharm_class_moa": ["DOPA Decarboxylase Inhibitors [MoA]"], "manufacturer_name": ["BluePoint Laboratories"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68001-172-00)", "package_ndc": "68001-172-00", "marketing_end_date": "20260228", "marketing_start_date": "20140122"}], "brand_name": "CARBIDOPA AND LEVODOPA", "product_id": "68001-172_304c30d1-a315-0451-e063-6294a90abb9f", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Amino Acids", "Aromatic [CS]", "Aromatic Amino Acid [EPC]"], "product_ndc": "68001-172", "generic_name": "Carbidopa and Levodopa", "labeler_name": "BluePoint Laboratories", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CARBIDOPA AND LEVODOPA", "active_ingredients": [{"name": "CARBIDOPA", "strength": "50 mg/1"}, {"name": "LEVODOPA", "strength": "200 mg/1"}], "application_number": "ANDA202323", "marketing_category": "ANDA", "marketing_end_date": "20260228", "marketing_start_date": "20140122"}