carbidopa and levodopa

Generic: carbidopa and levodopa

Labeler: radha 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 radha pharmaceuticals inc
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

carbidopa 25 mg/1, levodopa 100 mg/1

Manufacturer
Radha Pharmaceuticals Inc

Identifiers & Regulatory

Product NDC 77771-460
Product ID 77771-460_33a24383-bc09-1d2c-e063-6394a90af626
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA214091
Listing Expiration 2026-12-31
Marketing Start 2025-04-25

Pharmacologic Class

Established (EPC)
aromatic amino acid [epc] aromatic amino acid decarboxylation inhibitor [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 77771460
Hyphenated Format 77771-460

Supplemental Identifiers

RxCUI
308988 308989
UPC
0377771461010 0377771460013
UNII
46627O600J MNX7R8C5VO
NUI
N0000193220 M0370111 N0000175754 N0000175755

Packaging Origin

Original Packager
true

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 ANDA214091 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
  • 100 mg/1
source: ndc
Packaging
  • 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (77771-460-01)
source: ndc

Packages (1)

77771-460-01 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (77771-460-01)

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": "33a24383-bc09-1d2c-e063-6394a90af626", "openfda": {"nui": ["N0000193220", "M0370111", "N0000175754", "N0000175755"], "upc": ["0377771461010", "0377771460013"], "unii": ["46627O600J", "MNX7R8C5VO"], "rxcui": ["308988", "308989"], "spl_set_id": ["33a22ffe-0d41-162d-e063-6394a90a43d3"], "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": ["Radha Pharmaceuticals Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (77771-460-01)", "package_ndc": "77771-460-01", "marketing_start_date": "20250425"}], "brand_name": "Carbidopa and Levodopa", "product_id": "77771-460_33a24383-bc09-1d2c-e063-6394a90af626", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Amino Acids", "Aromatic [CS]", "Aromatic Amino Acid [EPC]"], "product_ndc": "77771-460", "generic_name": "Carbidopa and Levodopa", "labeler_name": "Radha 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": "ANDA214091", "marketing_category": "ANDA", "marketing_start_date": "20250425", "listing_expiration_date": "20261231"}