Details for New Drug Application (NDA): 050739

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NDA 050739 describes OMNICEF, which is a drug marketed by Abbvie and is included in two NDAs. Additional details are available on the OMNICEF profile page.

The generic ingredient in OMNICEF is cefdinir. There are twelve drug master file entries for this compound. Twenty-eight suppliers are listed for this compound. Additional details are available on the cefdinir profile page.

Summary for 050739

Tradename:	OMNICEF
Applicant:	Abbvie
Ingredient:	cefdinir
Patents:	0

Profile for product number 001

Active Rx/OTC/Discontinued:	DISCN	Dosage:	CAPSULE;ORAL			Strength	300MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons
Approval Date:	Dec 4, 1997	TE:		RLD:	Yes

Expired US Patents for NDA 050739

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Applicant	Tradename	Generic Name	Dosage	NDA	Approval Date	Patent No.	Patent Expiration
Abbvie	OMNICEF	cefdinir	CAPSULE;ORAL	050739-001	Dec 4, 1997	⤷ Sign Up	⤷ Sign Up
>Applicant	>Tradename	>Generic Name	>Dosage	>NDA	>Approval Date	>Patent No.	>Patent Expiration

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