🇺🇸
United States · US · US:68180-987_0098094d-a0c0-4b55-9851-68aaf0109233
DROXIDOPA
Orange BookUNIISPLATC C01CA27
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerLupin Pharmaceuticals, Inc.
CountryUS (United States)
ATC codeC01CA27
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 0
No packs registered.
Annotations
UNII (FDA Substance ID)
J7A92W69L7
DROXIDOPA
RxCUI 1489913
Orange Book
A211652
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "J7A92W69L7",
"rxcui": "1489913",
"inchikey": "QXWYKJLNLSIPIN-JGVFFNPUSA-N",
"display_name": "DROXIDOPA",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"381ffe44-d5d8-4380-a3cd-6d6a5e9ef55d": {
"match": "brand_token",
"title": "DROXIDOPA CAPSULE [NOVADOZ PHARMACEUTICALS LLC]",
"spl_version": "2",
"published_date": "2026-02-10"
}
},
"productid": "68180-987_0098094d-a0c0-4b55-9851-68aaf0109233",
"productndc": "68180-987",
"dosage_form": "CAPSULE",
"orange_book": {
"appl_no": "211652",
"products": [
{
"rs": false,
"rld": false,
"te_code": null,
"strength": "100MG",
"product_no": "001",
"approval_date": "Feb 18, 2021"
},
{
"rs": false,
"rld": false,
"te_code": null,
"strength": "200MG",
"product_no": "002",
"approval_date": "Feb 18, 2021"
},
{
"rs": false,
"rld": false,
"te_code": null,
"strength": "300MG",
"product_no": "003",
"approval_date": "Feb 18, 2021"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "DROXIDOPA",
"proprietary_name": "DROXIDOPA",
"active_ingred_unit": "mg/1",
"application_number": "ANDA211652",
"marketing_category": "ANDA",
"nonproprietary_name": "DROXIDOPA",
"start_marketing_date": "20210924",
"active_numerator_strength": "100"
}Related drugs
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