Details for New Drug Application (NDA): 085873

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NDA 085873 describes BUTABARB, which is a drug marketed by Alpharma Us Pharms, Bundy, Wockhardt, Sandoz, Solvay, Teva, Watson Labs, and Whiteworth Town Plsn, and is included in seventeen NDAs. Additional details are available on the BUTABARB profile page.

The generic ingredient in BUTABARB is butabarbital sodium. There are nine drug master file entries for this compound. Additional details are available on the butabarbital sodium profile page.

Summary for 085873

Tradename:	BUTABARB
Applicant:	Alpharma Us Pharms
Ingredient:	butabarbital sodium
Patents:	0

Profile for product number 001

Active Rx/OTC/Discontinued:	DISCN	Dosage:	ELIXIR;ORAL			Strength	30MG/5ML
Approval Date:	Approved Prior to Jan 1, 1982	TE:		RLD:	No

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