carbidopa and levodopa

Generic: carbidopa and levodopa

Labeler: dr. reddy's laboratories inc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name carbidopa and levodopa
Generic Name carbidopa and levodopa
Labeler dr. reddy's laboratories inc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

carbidopa 25 mg/1, levodopa 250 mg/1

Manufacturer
Dr. Reddy's Laboratories Inc

Identifiers & Regulatory

Product NDC 75907-021
Product ID 75907-021_79e0bfad-1855-2d1c-08df-991280a54eda
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA073607
Listing Expiration 2026-12-31
Marketing Start 2024-05-01

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 75907021
Hyphenated Format 75907-021

Supplemental Identifiers

RxCUI
197443 197444 197445
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 ANDA073607 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
  • 250 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (75907-021-01)
  • 500 TABLET in 1 BOTTLE (75907-021-05)
source: ndc

Packages (2)

75907-021-01 100 TABLET in 1 BOTTLE (75907-021-01) 75907-021-05 500 TABLET in 1 BOTTLE (75907-021-05)

Ingredients (2)

carbidopa (25 mg/1) levodopa (250 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": "79e0bfad-1855-2d1c-08df-991280a54eda", "openfda": {"nui": ["N0000193220", "M0370111", "N0000175754", "N0000175755"], "unii": ["46627O600J", "MNX7R8C5VO"], "rxcui": ["197443", "197444", "197445"], "spl_set_id": ["87ab55c9-203d-d595-3e3e-0e38f2f6d9c4"], "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": ["Dr. Reddy's Laboratories Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (75907-021-01)", "package_ndc": "75907-021-01", "marketing_start_date": "20240501"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (75907-021-05)", "package_ndc": "75907-021-05", "marketing_start_date": "20250315"}], "brand_name": "Carbidopa and Levodopa", "product_id": "75907-021_79e0bfad-1855-2d1c-08df-991280a54eda", "dosage_form": "TABLET", "pharm_class": ["Amino Acids", "Aromatic [CS]", "Aromatic Amino Acid [EPC]"], "product_ndc": "75907-021", "generic_name": "Carbidopa and Levodopa", "labeler_name": "Dr. Reddy's Laboratories Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Carbidopa and Levodopa", "active_ingredients": [{"name": "CARBIDOPA", "strength": "25 mg/1"}, {"name": "LEVODOPA", "strength": "250 mg/1"}], "application_number": "ANDA073607", "marketing_category": "ANDA", "marketing_start_date": "20240501", "listing_expiration_date": "20261231"}