NDC 31722-008 – Zafirlukast
Zafirlukast 20 mg/1 · Tablet, Film Coated · Oral
Product NDC31722-008
Product details
- Brand name
- Zafirlukast
- Generic name
- Zafirlukast
- Labeler
- Camber Pharmaceuticals, Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA212475
- Marketed since
- September 10, 2020
- Listing expires
- December 31, 2026
- Pharmacologic class
- Leukotriene Receptor Antagonist
Active ingredients
- Zafirlukast 20 mg/1
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 31722-008-01 | 10 BLISTER PACK in 1 CARTON (31722-008-01) / 10 TABLET, FILM COATED in 1 BLISTER PACK | Sep 10, 2020 |
| 31722-008-05 | 500 TABLET, FILM COATED in 1 BOTTLE (31722-008-05) | Sep 10, 2020 |
| 31722-008-60 | 60 TABLET, FILM COATED in 1 BOTTLE (31722-008-60) | Sep 10, 2020 |
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