NDC 47335-236 – Ambrisentan

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

Human Prescription Drug

Product NDC47335-236

Product details

Brand name
Ambrisentan
Generic name
Ambrisentan
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA210784
Marketed since
April 29, 2019
Listing expires
December 31, 2026
Pharmacologic class
Endothelin Receptor Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Ambrisentan →

Package NDC codes (4)

Package NDCDescriptionSince
47335-236-643 BLISTER PACK in 1 CARTON (47335-236-64) / 10 TABLET, FILM COATED in 1 BLISTER PACK (47335-236-60)Apr 29, 2019
47335-236-661 BLISTER PACK in 1 CARTON (47335-236-66) / 10 TABLET, FILM COATED in 1 BLISTER PACK (47335-236-60)Apr 29, 2019
47335-236-8330 TABLET, FILM COATED in 1 BOTTLE (47335-236-83)Apr 29, 2019
47335-236-8510 TABLET, FILM COATED in 1 BOTTLE (47335-236-85)Apr 29, 2019

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