Guaifenesin And Dextromethorphan Hbr Tablet, Extended Release
Product Images NDC 65162-039

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 6 technical images submitted to the FDA as part of the official labeling for Guaifenesin And Dextromethorphan Hbr (NDC 65162-039). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Amneal 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

1200mg Blister Pack (Guaifenesin And Dextromethorphan Hbr Extended Rele 1)

1200mg Blister Pack (Guaifenesin And Dextromethorphan Hbr Extended Rele 1)
Blister pack label for Maximum Strength Guaifenesin and Dextromethorphan HBr extended-release tablets, 1200 mg/60 mg strength. The label instructs to push tablets through foil and lists Amneal Pharmaceuticals LLC, Bridgewater, NJ, as the distributor. Lot and expiration date fields are present but not filled in.*
FDA Label Image

1200mg- 30ct Label (Guaifenesin And Dextromethorphan Hbr Extended Rele 2)

1200mg- 30ct Label (Guaifenesin And Dextromethorphan Hbr Extended Rele 2)
Label for Guaifenesin and Dextromethorphan HBr Extended-Release Tablets by Amneal Pharmaceuticals LLC. The product contains 1200 mg of guaifenesin and 60 mg of dextromethorphan HBr per tablet. The label states it is an expectorant and cough suppressant, with 30 extended-release tablets in the package. Directions for use and a barcode are visible.*
FDA Label Image

1200mg- 30ct Carton (Guaifenesin And Dextromethorphan Hbr Extended Rele 3)

1200mg- 30ct Carton (Guaifenesin And Dextromethorphan Hbr Extended Rele 3)
Label for Guaifenesin and Dextromethorphan HBr extended-release tablets, 1200 mg/60 mg strength, by Amneal Pharmaceuticals LLC. The label highlights this is a maximum strength expectorant and cough suppressant in a 30-count package. The design features drug facts and directions, active and inactive ingredients, warnings, and manufacturer information with barcode.*
FDA Label Image

1200mg- 60ct Label (Guaifenesin And Dextromethorphan Hbr Extended Rele 4)

1200mg- 60ct Label (Guaifenesin And Dextromethorphan Hbr Extended Rele 4)
Label for Guaifenesin and Dextromethorphan HBr Extended-Release Tablets, 1200 mg/60 mg, by Amneal Pharmaceuticals LLC. The label states it is an expectorant and cough suppressant, contains 60 extended-release tablets, and includes directions for use and a warning for parents about teen medicine abuse.*
FDA Label Image

1200mg- 60ct Carton (Guaifenesin And Dextromethorphan Hbr Extended Rele 5)

1200mg- 60ct Carton (Guaifenesin And Dextromethorphan Hbr Extended Rele 5)
Packaging label for Guaifenesin and Dextromethorphan HBr Extended-Release Tablets, 1200 mg/60 mg, from Amneal Pharmaceuticals LLC. The label highlights this product as maximum strength, designed as an expectorant and cough suppressant. It includes Drug Facts panels with active ingredients, uses, warnings, directions, and other information. The package indicates 60 extended-release tablets with dosing and safety information.*
FDA Label Image

1200 mg Blister Carton (Guaifenesin And Dextromethorphan Hbr Extended Rele 6)

1200 mg Blister Carton (Guaifenesin And Dextromethorphan Hbr Extended Rele 6)
Packaging label for Guaifenesin and Dextromethorphan HBr Extended-Release Tablets, maximum strength 1200 mg/60 mg. The label shows the product as expectorant and cough suppressant in a 20 extended-release tablet count carton. Distributed by Amneal Pharmaceuticals LLC, with a prominent red and purple design highlighting the dosage and product attributes.*

* 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.