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United States · US · US:0074-3012_3141c7d9-a3c8-4658-8a14-22182f452465
Duopa
Orange BookUNIISPLATC N04BA
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerAbbVie Inc.
CountryUS (United States)
ATC codeN04BA
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1100743012077 CARTRIDGE in 1 CARTON (0074-3012-07) / 100 mL in 1 CARTRIDGE
Annotations
UNII (FDA Substance ID)
MNX7R8C5VO
CARBIDOPA HYDRATE
RxCUI 2019
Orange Book
N203952
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "MNX7R8C5VO",
"rxcui": "2019",
"inchikey": "QTAOMKOIBXZKND-PPHPATTJSA-N",
"display_name": "CARBIDOPA HYDRATE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ENTERAL",
"spl_meta": {
"7066d371-dc6a-0d6f-7bed-e5dd4ee912da": {
"match": "brand_token",
"title": "DUOPA (CARBIDOPA AND LEVODOPA) SUSPENSION [ABBVIE INC.]",
"spl_version": "171",
"published_date": "2026-04-01"
}
},
"productid": "0074-3012_3141c7d9-a3c8-4658-8a14-22182f452465",
"productndc": "0074-3012",
"dosage_form": "SUSPENSION",
"orange_book": {
"appl_no": "203952",
"products": [
{
"rs": true,
"rld": true,
"te_code": null,
"strength": "4.63MG/ML;20MG/ML",
"product_no": "001",
"approval_date": "Jan 9, 2015"
}
],
"appl_type": "N"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "CARBIDOPA HYDRATE; LEVODOPA",
"proprietary_name": "Duopa",
"active_ingred_unit": "mg/mL; mg/mL",
"application_number": "NDA203952",
"marketing_category": "NDA",
"nonproprietary_name": "Carbidopa and Levodopa",
"start_marketing_date": "20150115",
"active_numerator_strength": "4.63; 20"
}Related drugs
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