NDC 55111-625 – Zafirlukast

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

Human Prescription Drug

Product NDC55111-625

Product details

Brand name
Zafirlukast
Generic name
Zafirlukast
Labeler
Dr. Reddys Laboratories Limited
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA090372
Marketed since
November 18, 2010
Listing expires
December 31, 2026
Pharmacologic class
Leukotriene Receptor Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Zafirlukast →

Package NDC codes (5)

Package NDCDescriptionSince
55111-625-01100 TABLET, FILM COATED in 1 BOTTLE (55111-625-01)Nov 18, 2010
55111-625-05500 TABLET, FILM COATED in 1 BOTTLE (55111-625-05)Nov 18, 2010
55111-625-3030 TABLET, FILM COATED in 1 BOTTLE (55111-625-30)Nov 18, 2010
55111-625-6060 TABLET, FILM COATED in 1 BOTTLE (55111-625-60)Nov 18, 2010
55111-625-7810 BLISTER PACK in 1 CARTON (55111-625-78) / 10 TABLET, FILM COATED in 1 BLISTER PACK (55111-625-79)Nov 18, 2010

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