NDC 61958-0801 – Letairis

Ambrisentan 5 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC61958-0801

Product details

Brand name
Letairis
Generic name
Ambrisentan
Labeler
Gilead Sciences, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
NDA · NDA022081
Marketed since
June 15, 2007
Listing expires
December 31, 2027
Pharmacologic class
Endothelin Receptor Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Letairis →

Package NDC codes (6)

Package NDCDescriptionSince
61958-0801-130 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (61958-0801-1)Jun 15, 2007
61958-0801-23 BLISTER PACK in 1 CARTON (61958-0801-2) / 10 TABLET, FILM COATED in 1 BLISTER PACKJun 15, 2007
61958-0801-31 BLISTER PACK in 1 CARTON (61958-0801-3) / 10 TABLET, FILM COATED in 1 BLISTER PACKJun 15, 2007
61958-0801-41 BLISTER PACK in 1 CARTON (61958-0801-4) / 10 TABLET, FILM COATED in 1 BLISTER PACKJun 15, 2007
61958-0801-510 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (61958-0801-5)Jun 15, 2007
61958-0801-610 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (61958-0801-6)Jun 15, 2007

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