NDC 82773-003-02 - 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
Requested NDC: 82773-003-02
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

Reported adverse events (FAERS/openFDA)#

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