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United States · US · US:72888-192_f2ff4283-6a46-451e-9a9e-e7090ecf2b3a
MYCOPHENOLATE MOFETIL
Orange BookUNIISPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerAdvagen Pharma Limited
CountryUS (United States)
ATC code—
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc117288819201100 CAPSULE in 1 BOTTLE (72888-192-01)
- ndc117288819205500 CAPSULE in 1 BOTTLE (72888-192-05)
Annotations
UNII (FDA Substance ID)
9242ECW6R0
MYCOPHENOLATE MOFETIL
RxCUI 68149
Orange Book
A210181
AB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "9242ECW6R0",
"rxcui": "68149",
"inchikey": "RTGDFNSFWBGLEC-SYZQJQIISA-N",
"display_name": "MYCOPHENOLATE MOFETIL",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"21ff53b0-b4ba-4473-91e4-76ef41681064": {
"match": "brand_token",
"title": "MYCOPHENOLATE MOFETIL POWDER, FOR SUSPENSION [ASCEND LABORATORIES, LLC]",
"spl_version": "30",
"published_date": "2026-05-28"
}
},
"productid": "72888-192_f2ff4283-6a46-451e-9a9e-e7090ecf2b3a",
"productndc": "72888-192",
"dosage_form": "CAPSULE",
"orange_book": {
"appl_no": "210181",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "250MG",
"product_no": "001",
"approval_date": "Jan 8, 2019"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "MYCOPHENOLATE MOFETIL",
"proprietary_name": "MYCOPHENOLATE MOFETIL",
"active_ingred_unit": "mg/1",
"application_number": "ANDA210181",
"marketing_category": "ANDA",
"nonproprietary_name": "MYCOPHENOLATE MOFETIL",
"start_marketing_date": "20230801",
"active_numerator_strength": "250"
}Access this data programmatically
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