carbidopa and levodopa

Generic: carbidopa and levodopa

Labeler: zydus pharmaceuticals usa inc.
NDC Directory HUMAN PRESCRIPTION DRUG NDA AUTHORIZED GENERIC Inactive Finished

Drug Facts

Product Profile

Brand Name carbidopa and levodopa
Generic Name carbidopa and levodopa
Labeler zydus pharmaceuticals usa inc.
Dosage Form CAPSULE, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

carbidopa 48.75 mg/1, levodopa 195 mg/1

Manufacturer
Zydus Pharmaceuticals USA Inc.

Identifiers & Regulatory

Product NDC 70710-2141
Product ID 70710-2141_9f66a828-7712-41a2-8380-682a3bbe50d6
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA AUTHORIZED GENERIC
Application Number NDA203312
Listing Expiration 2026-12-31
Marketing Start 2025-10-20

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 707102141
Hyphenated Format 70710-2141

Supplemental Identifiers

RxCUI
1600773 1600775 1600914 1600916
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 NDA203312 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 48.75 mg/1
  • 195 mg/1
source: ndc
Packaging
  • 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70710-2141-1)
source: ndc

Packages (1)

70710-2141-1 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70710-2141-1)

Ingredients (2)

carbidopa (48.75 mg/1) levodopa (195 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": "9f66a828-7712-41a2-8380-682a3bbe50d6", "openfda": {"nui": ["N0000193220", "M0370111", "N0000175754", "N0000175755"], "unii": ["46627O600J", "MNX7R8C5VO"], "rxcui": ["1600773", "1600775", "1600914", "1600916"], "spl_set_id": ["74e7f96b-de31-4e3c-b32d-11421b291d4e"], "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": ["Zydus Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70710-2141-1)", "package_ndc": "70710-2141-1", "marketing_start_date": "20251020"}], "brand_name": "Carbidopa and Levodopa", "product_id": "70710-2141_9f66a828-7712-41a2-8380-682a3bbe50d6", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Amino Acids", "Aromatic [CS]", "Aromatic Amino Acid [EPC]"], "product_ndc": "70710-2141", "generic_name": "Carbidopa and Levodopa", "labeler_name": "Zydus Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Carbidopa and Levodopa", "active_ingredients": [{"name": "CARBIDOPA", "strength": "48.75 mg/1"}, {"name": "LEVODOPA", "strength": "195 mg/1"}], "application_number": "NDA203312", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20251020", "listing_expiration_date": "20261231"}