Albuterol
Active substance: albuterol
TABLET · ALBUTEROL SULFATE 4 mg/1
United StatesActive
Marketing holder: Zydus Lifesciences Limited
Verified 2026-10-09 · openFDA NDC
- Source: openFDA NDC
Composition
- ALBUTEROL SULFATE · 4 mg/1
Registration
- Registration number
- 70771-1512
- Registration status
- Active
- Dispensing
- Prescription only
- Route
- ORAL
Sources
- product · openFDA NDC · 70771-1512 · Verified 2026-10-09 · open in source
- registration_status · openFDA NDC · 70771-1512 · Verified 2026-10-09 · open in source
- ingredients.0 · openFDA NDC · 70771-1512 · Verified 2026-10-09 · open in source