Details for New Drug Application (NDA): 020191

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NDA 020191 describes ALOMIDE, which is a drug marketed by Novartis and is included in one NDA. It is available from one supplier. Additional details are available on the ALOMIDE profile page.

The generic ingredient in ALOMIDE is lodoxamide tromethamine. One supplier is listed for this compound. Additional details are available on the lodoxamide tromethamine profile page.

Summary for 020191

Tradename:	ALOMIDE
Applicant:	Novartis
Ingredient:	lodoxamide tromethamine
Patents:	0

Pharmacology for NDA: 020191

Physiological Effect	Decreased Histamine Release

Suppliers and Packaging for NDA: 020191

Tradename	Generic Name	Dosage	NDA	Application Type	Supplier	National Drug Code	Package Code	Package
ALOMIDE	lodoxamide tromethamine	SOLUTION/DROPS;OPHTHALMIC	020191	NDA	Novartis Pharmaceuticals Corporation	0078-0736	0078-0736-10	1 BOTTLE in 1 CARTON (0078-0736-10) / 10 mL in 1 BOTTLE

Profile for product number 001

Active Rx/OTC/Discontinued:	RX	Dosage:	SOLUTION/DROPS;OPHTHALMIC			Strength	EQ 0.1% BASE
Approval Date:	Sep 23, 1993	TE:		RLD:	Yes

Expired US Patents for NDA 020191

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Applicant	Tradename	Generic Name	Dosage	NDA	Approval Date	Patent No.	Patent Expiration
Novartis	ALOMIDE	lodoxamide tromethamine	SOLUTION/DROPS;OPHTHALMIC	020191-001	Sep 23, 1993	⤷ Sign Up	⤷ Sign Up
>Applicant	>Tradename	>Generic Name	>Dosage	>NDA	>Approval Date	>Patent No.	>Patent Expiration

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