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United States · US · US:68682-200_ccf10efe-4fda-40a4-8f20-1ccefb151a15
Carbidopa
Orange BookSPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerOceanside Pharmaceuticals
CountryUS (United States)
ATC code—
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc116868220025100 TABLET in 1 BOTTLE (68682-200-25)
Annotations
Orange Book
N017830
AB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"route": "ORAL",
"spl_meta": {
"87ab55c9-203d-d595-3e3e-0e38f2f6d9c4": {
"match": "brand_token",
"title": "CARBIDOPA AND LEVODOPA TABLET [DR. REDDY'S LABORATORIES INC]",
"spl_version": "4",
"published_date": "2026-05-21"
}
},
"productid": "68682-200_ccf10efe-4fda-40a4-8f20-1ccefb151a15",
"productndc": "68682-200",
"dosage_form": "TABLET",
"orange_book": {
"appl_no": "017830",
"products": [
{
"rs": true,
"rld": true,
"te_code": "AB",
"strength": "25MG",
"product_no": "001",
"approval_date": "Approved Prior to Jan 1, 1982"
}
],
"appl_type": "N"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "CARBIDOPA",
"proprietary_name": "Carbidopa",
"active_ingred_unit": "mg/1",
"application_number": "NDA017830",
"marketing_category": "NDA AUTHORIZED GENERIC",
"nonproprietary_name": "Carbidopa Tablets",
"start_marketing_date": "20140404",
"active_numerator_strength": "25"
}Access this data programmatically
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