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
- 42571-464_3306ffee-e664-1534-e063-6294a90ad7ba
- Product NDC
- 42571-464
- Form
- SOLUTION
- Composition / generic term
- Arformoterol Tartrate
- Labeler
- Micro Labs Limited
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20250501
- 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 (42571-464-73) / 1 VIAL in 1 POUCH (42571-464-75) / 2 mL in 1 VIAL · 42571-464-73
Source and coverage
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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.
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