Home NDC 82773-003 NDC 82773-003 - Protirelin Acetate 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 82773-003
Package NDCs from labels 82773-003-02, 82773-003-01
Manufacturer Suzhou Qianyuan Biotechnology Co., Ltd.
Effective date 2022-11-30
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Labels# Label, Manufacturer, Effective date table Label Manufacturer Effective date Type Protirelin Acetate Suzhou Qianyuan Biotechnology Co., Ltd. 2022-11-30 BULK INGREDIENT - ANIMAL DRUG
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 82773-003-01 Protirelin Acetate 10 g in 1 JAR POWDER 10 1 82773-003-02 Protirelin Acetate 1 g in 1 VIAL POWDER 1 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 82773-003 PROTIRELIN ACETATE POWDER [SUZHOU QIANYUAN BIOTECHNOLOGY CO., LTD.] 1 2 package rows 20221202_fc1ace77-7dcb-4d98-bf69-a59073425923.zip