Carboplatin Injection, Solution
Product Images NDC 82511-006

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Carboplatin (NDC 82511-006). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Teyro Labs Private 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

Image (Carbo Inj Structure)

Chemical structure of carboplatin showing a platinum atom bonded to ammine groups and a cyclobutane dicarboxylate ligand. Molecular formula is C6H12N2O4Pt with a molecular weight of 371.25.*

FDA Label Image

Teyro-vial-label-15-ml (Carton Label 150mg)

Label for CARBOPLATIN Injection 150 mg/15 mL (10 mg/mL) multi-dose vial by Teyro Labs Private Limited. It is for intravenous use and is identified as a cytotoxic agent. The label includes storage instructions, manufacturer details, barcode, lot and expiration fields, and notes no preservatives are contained.*

FDA Label Image

Teyro-vial-45-ml (Carton Label 450mg)

CARBOPLATIN Injection 450 mg/45 mL (10 mg/mL) vial label showing a multi-dose vial for intravenous use. The label warns of cytotoxicity and indicates the product contains carboplatin USP in water for injection, is preservative-free, sterile, non-pyrogenic, and aqueous. Manufactured by Teyro Labs Private Limited, India, with storage instructions and barcode.*

FDA Label Image

Teyro-vial-label-5-ml (Carton Label 50mg)

CARBOplatin Injection 50 mg/5 mL (10 mg/mL) label for intravenous use by Teyro Labs Private Limited. The label includes a caution for cytotoxicity and states the product is a sterile, non-pyrogenic aqueous solution containing no preservatives. The packaging is for a 5 mL multi-dose vial and provides storage instructions, directions for dispensing by pharmacists, and manufacturer details in Tamil Nadu, India.*

FDA Label Image

Teyro-carton-label-60-ml (Carton Label 600mg)

CARBOPLATIN Injection (Aqueous Solution) 600 mg/60 mL (10 mg/mL) in a 60 mL multi-dose vial. Sterile aqueous solution for intravenous use. Label indicates cytotoxic agent with dispensing caution. Manufactured by Teyro Labs Private Limited, Tamil Nadu, India. Storage instructions include protecting from light and maintaining 20-25°C (68-77°F).*

FDA Label Image

Teyro-carton-15-ml (Container Label 150mg)

Label for CARBOPLATIN Injection 150 mg/15 mL (10 mg/mL) intravenous solution by Teyro Labs Private Limited. The packaging indicates a 15 mL multi-dose vial, labeled as a cytotoxic agent, with storage instructions and a reminder to read the accompanying package insert for complete directions. Manufactured in Tamil Nadu, India.*

FDA Label Image

Teyro-carton-label-45-ml (Container Label 450mg)

CARBOPlatin Injection 450 mg/45 mL (10 mg/mL) is an intravenous solution presented in a 45 mL multi-dose vial. The label indicates it is a cytotoxic agent and cautions pharmacists to dispense with an attached Patient Information Leaflet. The product is manufactured by Teyro Labs Private Limited, India, and is sterile, non-pyrogenic aqueous solution containing no preservatives.*

FDA Label Image

Teyro-carton-label-5-ml (Container Label 50mg)

Label for CARBOplatin Injection 50 mg/5 mL (10 mg/mL) solution for intravenous use. It is a 5 mL multi-dose vial labeled as a cytotoxic agent. The label includes storage instructions, manufacturer information (Teyro Labs Private Limited, India), and a barcode.*

FDA Label Image

Teyro-carton-label-60-ml (Container Label 600mg)

Label for CARBOPLATIN Injection Aqueous Solution 600 mg/60 mL (10 mg/mL) sterile intravenous injection in a 60 mL multi-dose vial. The label includes the NDC 82511-006-60, indicates no preservatives, cautions as a cytotoxic agent, and is manufactured by Teyro Labs Private Limited in India.*

* 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.