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
- 50742-394_36df181b-7f3a-3ad2-e063-6294a90ab756
- Product NDC
- 50742-394
- Form
- SOLUTION
- Composition / generic term
- Formoterol Fumarate
- Labeler
- Ingenus Pharmaceuticals, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20250605
- Source listing expiry
- 20261231
Source-listed ingredients
- FORMOTEROL FUMARATE — .02 mg/2mL
These values do not establish equivalence or a dose recommendation.
Packages
- 30 POUCH in 1 CARTON (50742-394-30) / 1 VIAL, SINGLE-DOSE in 1 POUCH (50742-394-01) / 2 mL in 1 VIAL, SINGLE-DOSE · 50742-394-30
- 60 POUCH in 1 CARTON (50742-394-60) / 1 VIAL, SINGLE-DOSE in 1 POUCH / 2 mL in 1 VIAL, SINGLE-DOSE · 50742-394-60
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 →