carbidopa and levodopa

Generic: carbidopa and levodopa

Labeler: nucare pharmaceuticals,inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name carbidopa and levodopa
Generic Name carbidopa and levodopa
Labeler nucare pharmaceuticals,inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

carbidopa 25 mg/1, levodopa 100 mg/1

Manufacturer
NuCare Pharmaceuticals,Inc.

Identifiers & Regulatory

Product NDC 68071-2240
Product ID 68071-2240_1d7656b4-b2d1-e4f7-e063-6394a90ab933
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078536
Listing Expiration 2026-12-31
Marketing Start 2008-10-28

Pharmacologic Class

Established (EPC)
aromatic amino acid decarboxylation inhibitor [epc] aromatic amino acid [epc]
Mechanism of Action
dopa decarboxylase inhibitors [moa]
Chemical Structure
amino acids, aromatic [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 680712240
Hyphenated Format 68071-2240

Supplemental Identifiers

RxCUI
197444
UPC
0368071224016
UNII
MNX7R8C5VO 46627O600J
NUI
N0000175754 N0000175755 N0000193220 M0370111

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name carbidopa and levodopa (source: ndc)
Generic Name carbidopa and levodopa (source: ndc)
Application Number ANDA078536 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
  • 100 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (68071-2240-1)
source: ndc

Packages (1)

68071-2240-1 100 TABLET in 1 BOTTLE (68071-2240-1)

Ingredients (2)

carbidopa (25 mg/1) levodopa (100 mg/1)

Linked Drug Pages (1)

CARBIDOPA AND LEVODOPA ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "1d7656b4-b2d1-e4f7-e063-6394a90ab933", "openfda": {"nui": ["N0000175754", "N0000175755", "N0000193220", "M0370111"], "upc": ["0368071224016"], "unii": ["MNX7R8C5VO", "46627O600J"], "rxcui": ["197444"], "spl_set_id": ["ad2ab0c4-188b-f025-e053-2a95a90a2816"], "pharm_class_cs": ["Amino Acids, Aromatic [CS]"], "pharm_class_epc": ["Aromatic Amino Acid Decarboxylation Inhibitor [EPC]", "Aromatic Amino Acid [EPC]"], "pharm_class_moa": ["DOPA Decarboxylase Inhibitors [MoA]"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (68071-2240-1)", "package_ndc": "68071-2240-1", "marketing_start_date": "20200818"}], "brand_name": "CARBIDOPA AND LEVODOPA", "product_id": "68071-2240_1d7656b4-b2d1-e4f7-e063-6394a90ab933", "dosage_form": "TABLET", "pharm_class": ["Amino Acids", "Aromatic [CS]", "Aromatic Amino Acid [EPC]"], "product_ndc": "68071-2240", "generic_name": "CARBIDOPA AND LEVODOPA", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CARBIDOPA AND LEVODOPA", "active_ingredients": [{"name": "CARBIDOPA", "strength": "25 mg/1"}, {"name": "LEVODOPA", "strength": "100 mg/1"}], "application_number": "ANDA078536", "marketing_category": "ANDA", "marketing_start_date": "20081028", "listing_expiration_date": "20261231"}