Theophylline Solution
Product Images NDC 0121-4820

4 FDA label images from Pai Holdings, Llc Dba Pai Pharma · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Theophylline (NDC 0121-4820). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Pai Holdings, Llc Dba Pai Pharma, 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

Theophylline Chemical Structure (Theophylline 01)

Theophylline Chemical Structure (Theophylline 01)
Chemical structure of the active ingredient Theophylline, showing its molecular framework with nitrogen and oxygen atoms and methyl groups attached, consistent with theophylline's known chemical formula.*
FDA Label Image

473 mL Bottle Label (Theophylline 02)

473 mL Bottle Label (Theophylline 02)
Theophylline Oral Solution USP 80 mg/15 mL label for an oral solution containing 20% alcohol. The label states storage instructions, dosage individualization, and prescription-only status. It lists the volume as 16 fl oz (473 mL) and is labeled by PAI Pharmaceutical Associates, Inc.*
FDA Label Image

118 mL Bottle Label (Theophylline 03)

118 mL Bottle Label (Theophylline 03)
The image shows a drug label for Theophylline Oral Solution USP, strength 80 mg/15 mL. The label states it contains 20% alcohol and is supplied in a 4 fl oz (118 mL) bottle. It includes storage instructions to keep at 20° to 25°C and directs dosage individualization. The label also advises dispensing in a child-resistant, light-resistant container and identifies the labeler as PAI Holdings, LLC dba PAI Pharma.*
FDA Label Image

15 mL Unit Dose Cup Label (Theophylline 04)

15 mL Unit Dose Cup Label (Theophylline 04)
Label for THEOPHYLLINE Oral Solution USP, 80 mg/15 mL, an oral solution human prescription drug. The label states a 20% alcohol content and a 15 mL delivery volume. It includes dosage warnings such as 'Package Not Child-Resistant' and 'Rx ONLY.' The label also displays the NDC number and the manufacturer, Pharmaceutical Associates, Inc., Greenville, SC.*

* 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.