Albuterol Sulfate Solution
Product Images NDC 65862-858

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 10 technical images submitted to the FDA as part of the official labeling for Albuterol Sulfate (NDC 65862-858). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Aurobindo Pharma Limited, 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

Twist The Cap Completely Off The Vial And Squeeze The Contents Into The Nebulizer Reservoir (Albuterol Fig1)

FDA Label Image

Connect The Nebulizer Reservoir To The Mouthpiece Or Face Mask (Albuterol Fig2)

FDA Label Image

Sit In A Comfortable, Upright Position; Place The Mouthpiece In Your Mouth (Albuterol Fig3)

FDA Label Image

Package Label-principal Display Panel (0.083% (2.5 mg/3 mL))

Package Label-principal Display Panel (0.083% (2.5 mg/3 mL))
This is a description of Albuterol Sulfate Inhalation Solution intended for oral inhalation only, not for injection. The potency is expressed as albuterol and each vial contains 2.5 mg/3 mL of the solution. The ingredients include albuterol, sodium chloride, edetate disodium, sodium citrate, hydrochloric acid, and water. The solution should be protected from light and stored in a pouch between 2-25°C. The usual dosage should be read on the accompanying insert and should be used only as directed by a physician. The solution is distributed by Aurobindo Pharma USA LLC and made in India.*
FDA Label Image

Package Label-principal Display Panel (0.083% (2.5 mg/3 mL))

Package Label-principal Display Panel (0.083% (2.5 mg/3 mL))
This is a description of a medication called Albuterol Sulfate Inhalation Solution. It contains 0.83 mg/mL of Albuterol as sulfate, along with sodium chloride, edetate disodium, sodium citrate (dihydrate), hydrochloric acid, and water for injection. The medication should be stored in a pouch until use, between 2° to 25°C (36° to 77°F) and protected from light. The usual dosage for the medication should be read from the accompanying insert and must only be used as directed by a physician without exceeding the recommended dosage. The medication is available in 3mL sterile unit-dose vials and is equivalent to 0.5 mL Albuterol Sulfate 0.5%*, which is diluted to 3mL with normal saline. The medication is for oral inhalation only, and not for injection. The medication is distributed by Aurobindo Pharma USA LLC and made in India.*
FDA Label Image

Package Label-principal Display Panel (0.083% (2.5 mg/3 mL))

Package Label-principal Display Panel (0.083% (2.5 mg/3 mL))
This is a product description for Albuterol Sulfate Inhalation Solution. The solution is for oral inhalation only and each vial contains 2.5mg/3mL of albuterol sulfate with potency expressed as albuterol. It is not for injection and contains inactive ingredients such as sodium chloride, edetate disodium, sodium citrate, hydrochloric acid and water for injection. The packaging comes with 30 sterile unit-dose vials, and patients receive an accompanying "Patient's Instruction for Use" from the pharmacist. The manufacturer is Aurobindo Pharma USA LLC, and the solution is made in India.*
FDA Label Image

Package Label-principal Display Panel (0.083% (2.5 mg/3 mL))

Package Label-principal Display Panel (0.083% (2.5 mg/3 mL))
This is a description of Albuterol Sulfate Inhalation Solution in a vial of 2.5 mg/3 mL potency expressed as Albuterol. It is used for oral inhalation only and not for injection. The vial contains 25 sterile unit doses and is equivalent to 0.5 mL of Albuterol Sulfate 0.5% diluted in normal saline. The package contains a patient's instruction for use, which should be dispensed by the pharmacist to every patient. The active ingredient in the inhalation solution is Albuterol (0.83 mg/mL) along with other inactive ingredients like sodium chloride, edetate disodium, sodium citrate, hydrochloric acid, and water for injection. It must be stored in the pouch until the time of use and kept between 2° to 25°C (36° to 77°F). It is made in India and distributed by Aurobindo Pharma USA LLC.*
FDA Label Image

Package Label-principal Display Panel (0.083% (2.5 mg/3 mL))

Package Label-principal Display Panel (0.083% (2.5 mg/3 mL))
This is a description of Albuterol sulfate inhalation solution which is used for oral inhalation only and not for injection. It is equivalent to 0.5 mL Albuterol Sulfate 0.5%. It comes in 30 vials of a sterile unit-dose. Pharmacists should dispense "Patient's Instruction for Use" to every user. The product should be kept in a pouch until it is ready to use and should be stored between 2° to 25°C (36° to 77°F) to protect it from light. The usual dosage should be read through the accompanying insert and should only be used with a physician's directive. The ingredients include albuterol as sulfate (0.83 mg/mL), sodium chloride, edetate disodium, sodium ctrate (diydrate), hydrochloric acid, and water for injection. The product is distributed by Aurobindo Pharma USA LLC, and it has a code of TS/DRUGS/13/2010.*
FDA Label Image

Package Label-principal Display Panel (0.083% (2.5 mg/3 mL))

Package Label-principal Display Panel (0.083% (2.5 mg/3 mL))
This is a label for Albuterol Sulfate Inhalation Solution, which is used for oral inhalation only and is not for injection. It is a sterile unit-dose vial and contains 2.5mg/3mL of Albuterol Sulfate. It is equivalent to 0.5mL of Albuterol Sulfate 0.5%, diluted to 3mL with normal saline. The usual dosage should be read in the accompanying insert. The label also includes instructions for the pharmacist to dispense the "Patient's Instruction for Use" to each patient. It is distributed by Aurobindo Pharma USA LLC and made in India.*
FDA Label Image

Chemical Structure (Albuterol Str)

Chemical Structure (Albuterol Str)
This text is not available as it contains only chemical symbols and cannot provide any context or useful description.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.