United States · FDA National Drug Code directory
arformoterol tartrate
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 43598-777_a718ab1b-b96b-bed2-24d1-b74c0277daed
- Product NDC
- 43598-777
- Form
- SOLUTION
- Composition / generic term
- arformoterol tartrate
- Labeler
- Dr. Reddy's Laboratories, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20240902
- Source listing expiry
- 20261231
Source-listed ingredients
- ARFORMOTEROL TARTRATE — 15 ug/2mL
These values do not establish equivalence or a dose recommendation.
Packages
- 30 POUCH in 1 CARTON (43598-777-30) / 1 VIAL, SINGLE-DOSE in 1 POUCH (43598-777-11) / 2 mL in 1 VIAL, SINGLE-DOSE · 43598-777-30
- 15 POUCH in 1 CARTON (43598-777-60) / 4 VIAL, SINGLE-DOSE in 1 POUCH (43598-777-48) / 2 mL in 1 VIAL, SINGLE-DOSE · 43598-777-60
Source and coverage
Open FDA National Drug Code directory →
Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
Browse United States records →