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United States · US · US:70710-2007_a3fd06db-9b81-4d16-a166-0e8b6bb2eccd
Deflazacort Oral Suspension
Orange BookUNIISPLATC H02AB13
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerZydus Pharmaceuticals (USA) Inc.
CountryUS (United States)
ATC codeH02AB13
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1170710200731 BOTTLE in 1 CARTON (70710-2007-3) / 13 mL in 1 BOTTLE
Annotations
UNII (FDA Substance ID)
KR5YZ6AE4B
DEFLAZACORT
RxCUI 22396
Orange Book
A220042
AB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "KR5YZ6AE4B",
"rxcui": "22396",
"inchikey": "FBHSPRKOSMHSIF-GRMWVWQJSA-N",
"display_name": "DEFLAZACORT",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"2fac1332-0247-1047-e063-6294a90a557f": {
"match": "brand_token",
"title": "DEFLAZACORT ORAL SUSPENSION (DEFLAZACORT ORAL) SUSPENSION [SUN PHARMACEUTICAL INDUSTRIES, INC.]",
"spl_version": "2",
"published_date": "2026-02-02"
}
},
"productid": "70710-2007_a3fd06db-9b81-4d16-a166-0e8b6bb2eccd",
"productndc": "70710-2007",
"dosage_form": "SUSPENSION",
"orange_book": {
"appl_no": "220042",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "22.75MG/ML",
"product_no": "001",
"approval_date": "Oct 3, 2025"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "DEFLAZACORT",
"proprietary_name": "Deflazacort Oral Suspension",
"active_ingred_unit": "mg/mL",
"application_number": "ANDA220042",
"marketing_category": "ANDA",
"nonproprietary_name": "Deflazacort",
"start_marketing_date": "20251023",
"active_numerator_strength": "22.75"
}Related drugs
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