United States · FDA National Drug Code directory
Formoterol fumarate
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
- 0093-4061_0ecd7fc0-7e29-4502-91ff-a0ead5a5a1f8
- Product NDC
- 0093-4061
- Form
- SOLUTION
- Composition / generic term
- Formoterol fumarate
- Labeler
- Teva Pharmaceuticals USA, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20210622
- Source listing expiry
- 20261231
Source-listed ingredients
- FORMOTEROL FUMARATE — 20 ug/2mL
These values do not establish equivalence or a dose recommendation.
Packages
- 60 POUCH in 1 CARTON (0093-4061-06) / 1 VIAL in 1 POUCH / 2 mL in 1 VIAL · 0093-4061-06
- 30 POUCH in 1 CARTON (0093-4061-30) / 1 VIAL in 1 POUCH (0093-4061-19) / 2 mL in 1 VIAL · 0093-4061-30
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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