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United States · US · US:23155-848_b5316b1d-ed7b-426d-9b86-dd17018c97a5
MYCOPHENOLATE MOFETIL
Orange BookUNIISPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerHeritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
CountryUS (United States)
ATC code—
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1123155848511 BOTTLE, PLASTIC in 1 CARTON (23155-848-51) / 225 mL in 1 BOTTLE, PLASTIC
Annotations
UNII (FDA Substance ID)
9242ECW6R0
MYCOPHENOLATE MOFETIL
RxCUI 68149
Orange Book
A212634
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": "23155-848_b5316b1d-ed7b-426d-9b86-dd17018c97a5",
"productndc": "23155-848",
"dosage_form": "POWDER, FOR SUSPENSION",
"orange_book": {
"appl_no": "212634",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "200MG/ML",
"product_no": "001",
"approval_date": "Aug 29, 2023"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "MYCOPHENOLATE MOFETIL",
"proprietary_name": "MYCOPHENOLATE MOFETIL",
"active_ingred_unit": "mg/mL",
"application_number": "ANDA212634",
"marketing_category": "ANDA",
"nonproprietary_name": "MYCOPHENOLATE MOFETIL",
"start_marketing_date": "20230905",
"active_numerator_strength": "200"
}Access this data programmatically
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