Zafirlukast
Active substance: zafirlukast
TABLET, FILM COATED · ZAFIRLUKAST 20 mg/1
United StatesActive
Marketing holder: Dr. Reddys Laboratories Limited
Verified 2026-10-09 · openFDA NDC
Analogues in other countries- Source: openFDA NDC
- Countries with the substance registered: 2
Composition
- ZAFIRLUKAST · 20 mg/1
Analogues by country
Products with the same active substance registered in other countries.
| Country | Products |
|---|---|
| RU 1 |
|
Import and control
Control by country
- Russiaprescription only
Source: GRLS (Russian state register) · record 01a120c4-d5b3-77dc-bc44-594d552a4d0a;count=1 · valid from 2026-10-09 · verified 2026-10-09
- United Statesprescription only
Source: openFDA NDC · record 01a1208c-75e4-7d69-b0e8-0ce08e2c054e,01a1208c-a549-70b5-8947-309f803d90b5,01a1208d-166f-7b1b-a9ae-0a00bb7e7861,01a1208e-8abc-7370-b6ad-c98e8a47e840,01a1208e-fec3-7ae9-b95f-388a178c6994;count=12 · valid from 2026-10-09 · verified 2026-10-09
Registration
- Registration number
- 55111-626
- Registration status
- Active
- Dispensing
- Prescription only
- Route
- ORAL
Sources
- product · openFDA NDC · 55111-626 · Verified 2026-10-09 · open in source
- registration_status · openFDA NDC · 55111-626 · Verified 2026-10-09 · open in source
- ingredients.0 · openFDA NDC · 55111-626 · Verified 2026-10-09 · open in source