NDC 55111-626 – Zafirlukast
Zafirlukast 20 mg/1 · Tablet, Film Coated · Oral
Product NDC55111-626
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
- Zafirlukast 20 mg/1
Package NDC codes (5)
| Package NDC | Description | Since |
|---|---|---|
| 55111-626-01 | 100 TABLET, FILM COATED in 1 BOTTLE (55111-626-01) | Nov 18, 2010 |
| 55111-626-05 | 500 TABLET, FILM COATED in 1 BOTTLE (55111-626-05) | Nov 18, 2010 |
| 55111-626-30 | 30 TABLET, FILM COATED in 1 BOTTLE (55111-626-30) | Nov 18, 2010 |
| 55111-626-60 | 60 TABLET, FILM COATED in 1 BOTTLE (55111-626-60) | Nov 18, 2010 |
| 55111-626-78 | 10 BLISTER PACK in 1 CARTON (55111-626-78) / 10 TABLET, FILM COATED in 1 BLISTER PACK (55111-626-79) | Nov 18, 2010 |
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