FDA DrugsClass II
methylprednisolone tablets, USP Dosepak, 4 mg, 1 Blister Card per Carton contain...
Published: February 4, 2026Recall ID: D-0299-2026Category: drugsCountry: US
Reason for Recall / Hazard
Labeling: Not Elsewhere Classified. Incorrect orientation of the blister foil applied to the blister cavities, which results in incorrect dosing information when following the directions on the foil.
Product Description & Identification
methylprednisolone tablets, USP Dosepak, 4 mg, 1 Blister Card per Carton containing 21 Tablets, Rx only, Distributed by: Greenstone LLC, Peapack, NJ 07977. NDC 59762-4440-2
Additional Source Details
| Field | Value |
|---|---|
| City | Peapack |
| State | NJ |
| Openfda › Nui › 1 | N0000175576 |
| Openfda › Nui › 2 | N0000175450 |
| Openfda › Upc › 1 | 0359762005014 |
| Openfda › Upc › 2 | 0359762005113 |
| Openfda › Upc › 3 | 0359762444035 |
| Openfda › Unii | X4W7ZR7023 |
| Openfda › Route | ORAL |
| Openfda › Spl id | bc3419a0-22a3-4eaf-a4f2-3133e9380663 |
| Openfda › Brand name | METHYLPREDNISOLONE |
| Openfda › Spl set id | 22dd75d6-f89a-44f7-8ca6-b64c4e9806dd |
| Openfda › Package ndc › 1 | 59762-4440-3 |
| Openfda › Package ndc › 2 | 59762-4440-2 |
| Openfda › Package ndc › 3 | 59762-0049-1 |
| Openfda › Package ndc › 4 | 59762-0050-1 |
| Openfda › Package ndc › 5 | 59762-0051-1 |
| Openfda › Product ndc › 1 | 59762-0049 |
| Openfda › Product ndc › 2 | 59762-4440 |
| Openfda › Product ndc › 3 | 59762-0050 |
| Openfda › Product ndc › 4 | 59762-0051 |
| Openfda › Generic name | METHYLPREDNISOLONE |
| Openfda › Product type | HUMAN PRESCRIPTION DRUG |
| Openfda › Substance name | METHYLPREDNISOLONE |
| Openfda › Pharm class epc | Corticosteroid [EPC] |
| Openfda › Pharm class moa | Corticosteroid Hormone Receptor Agonists [MoA] |
| Openfda › Manufacturer name | Mylan Pharmaceuticals Inc. |
| Openfda › Application number | NDA011153 |
| Openfda › Is original packager | true |
| Event id | 98278 |
| Address 1 | 100 Route 206 North |
| Address 2 | N/A |
| Code info | Lot # LG7675, Exp. Date Nov 2026 |
| Postal code | 07977 |
| Report date | 20260204 |
| Product type | Drugs |
| Product quantity | 3456 cartons |
| Reason for recall | Labeling: Not Elsewhere Classified. Incorrect orientation of the blister foil applied to the blister cavities, which results in incorrect dosing information when following the directions on the foil. |
| Voluntary mandated | Voluntary: Firm initiated |
| Recall initiation date | 20260115 |
| Initial firm notification | Letter |
| Center classification date | 20260128 |
Overview
- Recalling FirmGreenstone Llc
- StatusOngoing
- Risk LevelClass II
- DistributionNationwide within the United States