NDC 70771-1364 – Ambrisentan

Ambrisentan 10 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC70771-1364

Product details

Brand name
Ambrisentan
Generic name
Ambrisentan
Labeler
Zydus Lifesciences Limited
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA210058
Marketed since
April 12, 2019
Listing expires
December 31, 2026
Pharmacologic class
Endothelin Receptor Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Ambrisentan →

Package NDC codes (5)

Package NDCDescriptionSince
70771-1364-1100 TABLET, FILM COATED in 1 BOTTLE (70771-1364-1)Apr 12, 2019
70771-1364-330 TABLET, FILM COATED in 1 BOTTLE (70771-1364-3)Apr 12, 2019
70771-1364-71 BLISTER PACK in 1 CARTON (70771-1364-7) / 10 TABLET, FILM COATED in 1 BLISTER PACKApr 12, 2019
70771-1364-83 BLISTER PACK in 1 CARTON (70771-1364-8) / 10 TABLET, FILM COATED in 1 BLISTER PACKApr 12, 2019
70771-1364-990 TABLET, FILM COATED in 1 BOTTLE (70771-1364-9)Apr 12, 2019

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