NDC 68504-002 - GONABREED

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: 68504-002
Package NDCs from labels: 68504-002-01, 68504-002-02
Manufacturer: Parnell Technologies Pty Ltd
Effective date: 2025-11-05
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
GONABREED - Parnell Technologies Pty Ltd	Parnell Technologies Pty Ltd	2025-11-05	PRESCRIPTION ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
68504-002-01	GONABREED	1 in 1 CARTON	INJECTION, SOLUTION	1	8
68504-002-01	GONABREED	20 mL in 1 VIAL, MULTI-DOSE	INJECTION, SOLUTION	20	8
68504-002-02	GONABREED	100 mL in 1 VIAL, MULTI-DOSE	INJECTION, SOLUTION	100	8
68504-002-02	GONABREED	1 in 1 CARTON	INJECTION, SOLUTION	1	8

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
68504-002	GONABREED (GONADORELIN) INJECTION, SOLUTION [PARNELL TECHNOLOGIES PTY LTD]	7	4 package rows	20240829_9bc44a48-ff45-468a-a60d-c490a667d91d.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
GONADORELIN ACETATE	ACTIVE INGREDIENT	2RG1XQ1NYJ	GONABREED (GONADORELIN ACETATE) INJECTION, SOLUTION [PARNELL TECHNOLOGIES PTY LTD]	3
GONADORELIN	ACTIVE MOIETY	9O7312W37G	GONABREED (GONADORELIN ACETATE) INJECTION, SOLUTION [PARNELL TECHNOLOGIES PTY LTD]	3
BENZYL ALCOHOL	INACTIVE INGREDIENT	LKG8494WBH	GONABREED (GONADORELIN ACETATE) INJECTION, SOLUTION [PARNELL TECHNOLOGIES PTY LTD]	3
HYDROCHLORIC ACID	INACTIVE INGREDIENT	QTT17582CB	GONABREED (GONADORELIN ACETATE) INJECTION, SOLUTION [PARNELL TECHNOLOGIES PTY LTD]	3
SODIUM CHLORIDE	INACTIVE INGREDIENT	451W47IQ8X	GONABREED (GONADORELIN ACETATE) INJECTION, SOLUTION [PARNELL TECHNOLOGIES PTY LTD]	3
SODIUM HYDROXIDE	INACTIVE INGREDIENT	55X04QC32I	GONABREED (GONADORELIN ACETATE) INJECTION, SOLUTION [PARNELL TECHNOLOGIES PTY LTD]	3
SODIUM PHOSPHATE, DIBASIC	INACTIVE INGREDIENT	GR686LBA74	GONABREED (GONADORELIN ACETATE) INJECTION, SOLUTION [PARNELL TECHNOLOGIES PTY LTD]	3
SODIUM PHOSPHATE, MONOBASIC	INACTIVE INGREDIENT	3980JIH2SW	GONABREED (GONADORELIN ACETATE) INJECTION, SOLUTION [PARNELL TECHNOLOGIES PTY LTD]	3
water	INACTIVE INGREDIENT	059QF0KO0R	GONABREED (GONADORELIN ACETATE) INJECTION, SOLUTION [PARNELL TECHNOLOGIES PTY LTD]	3

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 56 of 56 · 1,104 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Join
SODIUM CHLORIDE	SODIUM CHLORIDE	Baxter Healthcare Corporation	b3b4b176-41f0-4ca8-90d4-3fba5707564a	2014-02-21	Exact identifier unii: 451W47IQ8X
TIS-U-SOL	SODIUM CHLORIDE, POTASSIUM CHLORIDE, MAGNESIUM SULFATE, SODIUM PHOSPHATE, AND POTASSIUM PHOSPHATE	Baxter Healthcare Corporation	9da4121f-d62d-4da4-8dfb-0494da16015f	2014-02-21	Exact identifier unii: 451W47IQ8X
Ringers	SODIUM CHLORIDE, CALCIUM CHLORIDE, POTASSIUM CHLORIDE,	Baxter Healthcare Corporation	e1953d54-818d-46a6-8532-518ebae6d84e	2012-06-13	Exact identifier unii: 451W47IQ8X
Lactated Ringers	SODIUM CHLORIDE, SODIUM LACTATE, POTASSIUM CHLORIDE, CALCIUM CHLORIDE	Baxter Healthcare Corporation	f09f80bf-2f8b-4420-865d-aec2d5e5cd4d	2012-06-12	Exact identifier unii: 451W47IQ8X

Reported adverse events (FAERS/openFDA)#

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