Oxycodone Hydrochloride Solution
Product Images NDC 70752-137

8 FDA label images from Quagen Pharmaceuticals Llc · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Oxycodone Hydrochloride (NDC 70752-137). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Quagen Pharmaceuticals Llc, 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

70752-137-03-carton (Carton100mg5ml30ml)

70752-137-03-carton (Carton100mg5ml30ml)
Packaging label for Oxycodone Hydrochloride Oral Solution USP 100 mg per 5 mL (20 mg per mL), manufactured by Quagen Pharmaceuticals LLC. The label includes dosage and usage instructions, storage conditions, a syringe measurement guide, cautionary statements, and details emphasizing use only in opioid-tolerant patients. The package size is 30 mL and the product is marked Rx Only, made in the USA.*
FDA Label Image

70752-136-10-carton (Carton5mg5ml100ml)

70752-136-10-carton (Carton5mg5ml100ml)
Carton label for Oxycodone Hydrochloride Oral Solution, USP 5 mg per 5 mL (1 mg per mL) by Quagen Pharmaceuticals LLC. The label specifies a 100 mL bottle, includes dosage strength, handling instructions, storage conditions, and a notice to use the enclosed measuring cup. The label features the Quagen Pharma logo and a Made in USA mark.*
FDA Label Image

70752-136-14-carton (Carton5mg5ml500ml)

70752-136-14-carton (Carton5mg5ml500ml)
Packaging label for Oxycodone Hydrochloride Oral Solution, USP 5 mg per 5 mL (1 mg per mL), manufactured by Quagen Pharmaceuticals LLC. The label includes dosage strength, volume of 500 mL, NDC 70752-136-14, storage instructions, and pharmacist dispensing guidance. It also notes the solution contains 0.05% alcohol and is made in the USA.*
FDA Label Image

Chemical Structure (Chemstructure)

Chemical Structure (Chemstructure)
Chemical structure of oxycodone hydrochloride, showing its molecular rings and functional groups along with the hydrochloride component.*
FDA Label Image

Figure1 (Figure1)

Figure1 (Figure1)
An instructional diagram of an oral dosing syringe for Oxycodone Hydrochloride solution. The syringe is labeled with volume and corresponding milligram doses up to 1 mL/20 mg. It includes a detailed zoomed-in section showing how to measure the dose from the widest portion of the plunger, with a caution not to measure at the narrow tip of the plunger.*
FDA Label Image

70752-137-03-label (Label100mg5ml30ml)

70752-137-03-label (Label100mg5ml30ml)
OXYCODONE HYDROCHLORIDE Oral Solution, USP 100 mg per 5 mL (20 mg per mL) in a 30 mL bottle. Label shows product name, strength, dosage form, directions for use only in patients who are opioid tolerant, manufacturer Quagen Pharmaceuticals LLC, and NDC 70752-137-03. The label includes storage and safety warnings and a barcode.*
FDA Label Image

70752-136-10-label (Label5mg5ml100ml)

70752-136-10-label (Label5mg5ml100ml)
Oxycodone Hydrochloride Oral Solution, USP 5 mg per 5 mL (1 mg per mL) in a 100 mL bottle. The label shows the product name prominently in red and black text, with a dosage strength highlight in a red box. The labeler is Quagen Pharmaceuticals LLC, West Caldwell, NJ. The label includes storage instructions and cautions to keep out of children’s reach, with an NDC number 70752-136-10.*
FDA Label Image

70752-136-14-label (Label5mg5ml500ml)

70752-136-14-label (Label5mg5ml500ml)
Oxycodone Hydrochloride Oral Solution USP 5 mg per 5 mL (1 mg per mL) in a 500 mL bottle, labeled by Quagen Pharmaceuticals LLC. The label includes dosage information, inactive ingredients, storage instructions, and a barcode. It is marked Rx Only and specifies dispensing with a medication guide.*

* 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.