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
62332-655_99e63a2d-5d11-43b4-ba83-1d64f3fc3914
Product NDC
62332-655
Form
SOLUTION
Composition / generic term
Formoterol Fumarate
Labeler
Alembic Pharmaceuticals Inc.
Marketing category
ANDA
Marketing start / end (source format)
20211122
Source listing expiry
20261231

Source-listed ingredients

  • FORMOTEROL FUMARATE — 20 ug/2mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 30 POUCH in 1 CARTON (62332-655-30) / 1 VIAL in 1 POUCH (62332-655-01) / 2 mL in 1 VIAL · 62332-655-30
  • 60 POUCH in 1 CARTON (62332-655-60) / 1 VIAL in 1 POUCH / 2 mL in 1 VIAL · 62332-655-60

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.

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Formoterol Fumarate — United States | Molindra Medicines