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United States · US · US:0009-0073_e4a8e5b4-af77-4eca-92de-cd0982969b82
Medrol
In shortageOrange BookUNIISPLATC H02BX01
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerPharmacia & Upjohn Company LLC
CountryUS (United States)
ATC codeH02BX01
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc11000900730150 TABLET in 1 BOTTLE (0009-0073-01)
Annotations
UNII (FDA Substance ID)
X4W7ZR7023
METHYLPREDNISOLONE
RxCUI 6902
Orange Book
N011153
ABABABAB
DailyMed SPL labels
1 version tracked
FDA shortage
Currently in shortage
Methylprednisolone Acetate Injection
Raw payload (JSON)
{
"unii": {
"unii": "X4W7ZR7023",
"rxcui": "6902",
"inchikey": "VHRSUDSXCMQTMA-PJHHCJLFSA-N",
"display_name": "METHYLPREDNISOLONE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"39d5270b-d957-4821-93d6-501b7b9f02d4": {
"match": "brand_token",
"title": "MEDROL (METHYLPREDNISOLONE) TABLET [PHARMACIA & UPJOHN COMPANY LLC]",
"spl_version": "25",
"published_date": "2025-11-18"
}
},
"productid": "0009-0073_e4a8e5b4-af77-4eca-92de-cd0982969b82",
"productndc": "0009-0073",
"dosage_form": "TABLET",
"orange_book": {
"appl_no": "011153",
"products": [
{
"rs": false,
"rld": true,
"te_code": "AB",
"strength": "4MG",
"product_no": "001",
"approval_date": "Approved Prior to Jan 1, 1982"
},
{
"rs": false,
"rld": true,
"te_code": null,
"strength": "2MG",
"product_no": "002",
"approval_date": "Approved Prior to Jan 1, 1982"
},
{
"rs": false,
"rld": true,
"te_code": "AB",
"strength": "16MG",
"product_no": "003",
"approval_date": "Approved Prior to Jan 1, 1982"
},
{
"rs": false,
"rld": true,
"te_code": "AB",
"strength": "8MG",
"product_no": "004",
"approval_date": "Approved Prior to Jan 1, 1982"
},
{
"rs": false,
"rld": false,
"te_code": null,
"strength": "24MG",
"product_no": "005",
"approval_date": "Approved Prior to Jan 1, 1982"
},
{
"rs": true,
"rld": true,
"te_code": "AB",
"strength": "32MG",
"product_no": "006",
"approval_date": "Approved Prior to Jan 1, 1982"
}
],
"appl_type": "N"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "METHYLPREDNISOLONE",
"shortage_reason": "Methylprednisolone Acetate Injection",
"shortage_status": "current",
"proprietary_name": "Medrol",
"active_ingred_unit": "mg/1",
"application_number": "NDA011153",
"marketing_category": "NDA",
"nonproprietary_name": "methylprednisolone",
"start_marketing_date": "19571024",
"active_numerator_strength": "16"
}Related drugs
Other records sharing ATC code H02BX01.
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