NDC 0061-0100 - Gentocin Durafilm

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: 0061-0100
Package NDCs from labels: 0061-0100-01
Manufacturer: Merck Sharp & Dohme Corp.
Effective date: 2024-11-15
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Gentocin Durafilm - Merck Sharp & Dohme Corp.	Merck Sharp & Dohme Corp.	2024-11-15	PRESCRIPTION ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
0061-0100-01	Gentocin Durafilm	1 in 1 CARTON	SOLUTION	1		6
0061-0100-01	Gentocin Durafilm	5 mL in 1 BOTTLE, DROPPER	SOLUTION	5		6

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
0061-0100	GENTOCIN DURAFILM (GENTAMICIN SULFATE AND BETAMETHASONE ACETATE) SOLUTION [MERCK SHARP & DOHME CORP.]	6	2 package rows	20241116_751e4b05-7d0e-4e7b-81d0-770a1edc2f76.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
BETAMETHASONE ACETATE	ACTIVE INGREDIENT	TI05AO53L7	GENTOCIN DURAFILM (GENTAMICIN SULFATE AND BETAMETHASONE ACETATE) SOLUTION [MERCK SHARP & DOHME CORP.]	1
GENTAMICIN SULFATE	ACTIVE INGREDIENT	8X7386QRLV	GENTOCIN DURAFILM (GENTAMICIN SULFATE AND BETAMETHASONE ACETATE) SOLUTION [MERCK SHARP & DOHME CORP.]	1
BETAMETHASONE	ACTIVE MOIETY	9842X06Q6M	GENTOCIN DURAFILM (GENTAMICIN SULFATE AND BETAMETHASONE ACETATE) SOLUTION [MERCK SHARP & DOHME CORP.]	1
GENTAMICIN	ACTIVE MOIETY	T6Z9V48IKG	GENTOCIN DURAFILM (GENTAMICIN SULFATE AND BETAMETHASONE ACETATE) SOLUTION [MERCK SHARP & DOHME CORP.]	1

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 3 of 3 · 47 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Betaloan SUIK	BETAMETHASONE SODIUM PHOSPHATE AND BETAMETHASONE ACETATE	Asclemed USA, Inc.	aec36d73-d753-4690-9e0e-a8ac7610855e	2022-10-12	Warnings, Adverse reactions	Exact identifier unii: TI05AO53L7
Gentamicin Sulfate	GENTAMICIN SULFATE	Asclemed USA, Inc.	b59e49e0-640b-43c3-ad07-711d1bb154e9	2022-07-19	Warnings, Adverse reactions	Exact identifier unii: 8X7386QRLV
Gentamicin Sulfate	GENTAMICIN SULFATE	Proficient Rx LP	3a6677a6-def5-443e-82bc-c185d41f03b7	2022-06-01	Warnings, Adverse reactions	Exact identifier unii: 8X7386QRLV
Gentamicin Sulfate	GENTAMICIN SULFATE	Asclemed USA, Inc.	a54e5c95-609d-4d66-9573-5d1ac78fa58f	2022-03-04	Warnings, Adverse reactions	Exact identifier unii: 8X7386QRLV
Gentamicin Sulfate	GENTAMICIN SULFATE	Proficient Rx LP	cf4386ba-c62a-4ee8-ab59-1bb2e737a5da	2021-05-01	Adverse reactions	Exact identifier unii: 8X7386QRLV
Gentak	GENTAMICIN SULFATE	Proficient Rx LP	aebfe247-cdf7-4acb-97b3-6d4341d7c815	2019-11-01	Warnings, Adverse reactions	Exact identifier unii: 8X7386QRLV
Gentamicin Sulfate	GENTAMICIN SULFATE	Proficient Rx LP	2098faaa-7f60-4640-8c37-19456ebba653	2019-11-01	Warnings, Adverse reactions	Exact identifier unii: 8X7386QRLV

Reported adverse events (FAERS/openFDA)#

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