Flower-symbol (Flower Symbol)
Folotyn Injection
Product Images NDC 72893-005
6 FDA label images from Acrotech Biopharma Inc · 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 Folotyn (NDC 72893-005). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Acrotech Biopharma 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.
Structural Formula (Image 01)
Chemical structure of pralatrexate, the active ingredient in Folotyn. The diagram shows the molecular arrangement with carbon, hydrogen, oxygen, nitrogen atoms, and bonds including specific functional groups characteristic of pralatrexate.*
Folotyn 20 mg/ml Carton (Image 02)
Carton packaging label for Folotyn (pralatrexate injection) 20 mg/mL, a human prescription intravenous injection. The label indicates a 1 mL vial and includes dosage form, strength, storage instructions, and manufacturer information for Acrotech Biopharma LLC. The label features barcodes and standard drug storage warnings.*
Folotyn 40 mg/ml Carton (Image 03)
Packaging label for Folotyn (pralatrexate injection) 40 mg/2 mL (20 mg/mL) intravenous injection. The label includes dosage strength, directions for use, handling instructions, NDC code, manufacturer information (Acrotech Biopharma LLC), and a barcode. The label indicates the product is for prescription use and provides storage instructions.*
Folotyn 20 mg/ml Vial (Image 04)
Label for Folotyn (pralatrexate injection) showing 20 mg/mL strength in a 1 mL vial. The label includes the Rx only designation and is manufactured by Acrotech Biopharma Inc. Instructions indicate not to dilute before intravenous injection.*
Folotyn 20 mg/ml Vial (Image 05)
Label for Folotyn (pralatrexate injection) 40 mg/2 mL (20 mg/mL) intravenous injection by Acrotech Biopharma Inc. The label indicates the product should not be diluted and is for prescription use only. It includes an NDC number, barcode, and a QR code.*
* 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.
