NDC 82712-2004-2 - Oclacitinib Maleate

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC
82712-2004
Requested NDC
82712-2004-2
Package NDCs from labels
82712-2004-2, 82712-2004-1, 82712-2004-3
Manufacturer
Sichuan Qingmu Pharmaceutical Co., Ltd.
Effective date
2026-04-22
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Oclacitinib Maleate - Sichuan Qingmu Pharmaceutical Co., Ltd.Sichuan Qingmu Pharmaceutical Co., Ltd.2026-04-22BULK INGREDIENT - ANIMAL DRUG
Oclacitinib Maleate - Sichuan Qingmu Pharmaceutical Co., Ltd.Sichuan Qingmu Pharmaceutical Co., Ltd.2026-01-05BULK INGREDIENT - ANIMAL DRUG
Oclacitinib Maleate - Sichuan Qingmu Pharmaceutical Co., Ltd.Sichuan Qingmu Pharmaceutical Co., Ltd.2026-01-05BULK INGREDIENT - ANIMAL DRUG

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
82712-2004-1Oclacitinib Maleate5 kg in 1 BAGPOWDER53
82712-2004-2Oclacitinib Maleate1 kg in 1 BAGPOWDER13
82712-2004-3Oclacitinib Maleate0.1 kg in 1 BAGPOWDER0.13

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.