Formoterol Fumarate Solution
Product Images NDC 62332-655

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Formoterol Fumarate (NDC 62332-655). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Alembic Pharmaceuticals Inc., these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

30s Pack Label

30s Pack Label
Packaging label for Formoterol Fumarate inhalation solution 20 mcg/2 mL vial by Alembic Pharmaceuticals Inc. The carton includes patient information, storage conditions, and usage instructions. The label specifies the solution is for oral inhalation only and contains 30 individually wrapped 2 mL single-dose vials.*
FDA Label Image

60s Pack Label

60s Pack Label
Packaging label for Formoterol Fumarate inhalation solution, 20 mcg / 2 mL vial, by Alembic Pharmaceuticals Inc. The carton indicates sterile unit dose vials, individually wrapped for oral inhalation only, with 60 vials per carton. Storage instructions and ingredients including active Formoterol fumarate and inactives are listed. The label also includes directions for healthcare providers and patients.*
FDA Label Image

Formoterol-figure-1 (Formoterol Figure 1)

Formoterol-figure-1 (Formoterol Figure 1)
Line graph titled 'Mean FEV1 at Day 1' showing lung function over 12 hours. It compares Formoterol Fumarate Inhalation Solution 20 mcg with placebo, plotting mean FEV1 in liters on the vertical axis against time in hours on the horizontal axis. The chart highlights higher FEV1 values for Formoterol versus placebo throughout the period.*
FDA Label Image

Formoterol-figure-2 (Formoterol Figure 2)

Formoterol-figure-2 (Formoterol Figure 2)
A line graph showing mean FEV1 in liters over 12 hours after 12 weeks of treatment comparing Formoterol Fumarate Inhalation Solution 20 mcg (N=123) and placebo (N=114). The Formoterol Fumarate line peaks higher than placebo throughout the time period shown.*
FDA Label Image

Formoterol-instruction-image-1 (Formoterol Instruction Image 1)

Formoterol-instruction-image-1 (Formoterol Instruction Image 1)
An instructional diagram showing a person using a pen-like inhaler device to dispense Formoterol Fumarate solution into a small nebulizer cup or reservoir. The illustration highlights the step of placing the inhaler tip into the nebulizer for respiratory inhalation use.*
FDA Label Image

Formoterol-instruction-image-2 (Formoterol Instruction Image 2)

Formoterol-instruction-image-2 (Formoterol Instruction Image 2)
An instructional diagram showing how to attach a nasal spray nozzle to the top of a spray bottle. A hand holds the spray bottle while another hand aligns the nozzle for attachment.*
FDA Label Image

Formoterol-instruction-image-3 (Formoterol Instruction Image 3)

Formoterol-instruction-image-3 (Formoterol Instruction Image 3)
Instructional illustration showing the use of a Formoterol Fumarate inhalation solution device. Two panels depict a person using the inhaler: one demonstrating inhalation through a mouthpiece and the other using a spacer or mask attachment for respiratory administration.*
FDA Label Image

Formoterol-structure (Formoterol Structure)

Formoterol-structure (Formoterol Structure)
Chemical structure diagram of Formoterol Fumarate dihydrate showing the molecular components including aromatic rings, hydroxyl groups, and the fumarate counterion with associated water molecules.*
FDA Label Image

Pouch Label

Pouch Label
The label displays Formoterol Fumarate inhalation solution in a 20 mcg/2 mL sterile unit-dose vial for oral inhalation. It includes active and inactive ingredient details, storage conditions, and safety instructions. Manufactured for Alembic Pharmaceuticals Inc., the label shows the NDC 62332-655-01 and states the product is Rx only with one unit dose vial per package.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.