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United States · US · US:62332-681_1b130bfa-78ff-40d2-8612-90e7133d2379
Albendazole
Orange BookUNIISPLATC P02CA03
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerAlembic Pharmaceuticals Inc.
CountryUS (United States)
ATC codeP02CA03
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc1162332681022 TABLET, FILM COATED in 1 BOTTLE (62332-681-02)
- ndc11623326812828 TABLET, FILM COATED in 1 BOTTLE (62332-681-28)
Annotations
UNII (FDA Substance ID)
F4216019LN
ALBENDAZOLE
RxCUI 430
Orange Book
A215652
AB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "F4216019LN",
"rxcui": "430",
"inchikey": "HXHWSAZORRCQMX-UHFFFAOYSA-N",
"display_name": "ALBENDAZOLE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"8de337eb-92e1-15b5-e053-2a95a90ac4f1": {
"match": "brand_token",
"title": "ALBENDAZOLE TABLET [GOLDEN STATE MEDICAL SUPPLY, INC.]",
"spl_version": "4",
"published_date": "2026-02-06"
}
},
"productid": "62332-681_1b130bfa-78ff-40d2-8612-90e7133d2379",
"productndc": "62332-681",
"dosage_form": "TABLET, FILM COATED",
"orange_book": {
"appl_no": "215652",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "200MG",
"product_no": "001",
"approval_date": "Sep 4, 2024"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "ALBENDAZOLE",
"proprietary_name": "Albendazole",
"active_ingred_unit": "mg/1",
"application_number": "ANDA215652",
"marketing_category": "ANDA",
"nonproprietary_name": "Albendazole",
"start_marketing_date": "20240911",
"active_numerator_strength": "200"
}Related drugs
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