Paricalcitol Injection
Product Images NDC 70121-1033

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Paricalcitol (NDC 70121-1033). 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

1 (Paricalcitol Injection 1)

Chemical structure diagram of paricalcitol, showing its molecular layout with rings, hydroxyl groups, and side chains as part of its steroidal framework.*

FDA Label Image

2 (Paricalcitol Injection 2)

Label for Paricalcitol Injection, USP 2 mcg/mL single-dose vial for intravenous use. Each mL contains paricalcitol 2 mcg, with propylene glycol 30% and alcohol 20%. Distributed by Amneal Pharmaceutical LLC, Bridgewater, NJ, manufactured in India. Includes NDC barcode and note: Rx only.*

FDA Label Image

3 (Paricalcitol Injection 3)

Paricalcitol Injection, USP 2 mcg/mL single-dose vials packaging label. The label states the product is sterile, non-pyrogenic, for intravenous use, and comes in 10 x 1 mL single-dose vials. Manufactured by Amneal Pharmaceuticals Pvt. Ltd. and distributed by Amneal Pharmaceuticals LLC. Instructions note to discard unused portions and use aseptic technique. Contains barcode and storage instructions.*

FDA Label Image

4 (Paricalcitol Injection 4)

Paricalcitol Injection, USP 5 mcg/mL single-dose vial label. The label indicates intravenous use and a 1 mL vial size. It lists excipients including propylene glycol 30% and alcohol 20%, and states the product is made in India and distributed by Amneal Pharmaceuticals LLC.*

FDA Label Image

5 (Paricalcitol Injection 5)

Label for Paricalcitol Injection USP 5 mcg/mL single-dose vials by Amneal Pharmaceuticals. The injection is sterile, non-pyrogenic, for intravenous use only, packaged as 10 x 1 mL vials. Manufactured in India and distributed by Amneal Pharmaceuticals LLC, Bridgewater, NJ. The label includes storage instructions, use aseptic technique, and a barcode.*

FDA Label Image

6 (Paricalcitol Injection 6)

Label for Paricalcitol Injection, USP 10 mcg/2 mL (5 mcg/mL) single-dose vial. The intravenous injection contains paricalcitol 5 mcg per mL with excipients including propylene glycol and alcohol. Distributed by Amneal Pharmaceuticals LLC, Bridgewater, NJ. The label includes NDC 70121-1035-1 and indicates Rx only.*

FDA Label Image

7 (Paricalcitol Injection 7)

Paricalcitol Injection, USP 10 mcg/2 mL (5 mcg/mL) intravenous injection single-dose vial carton by Amneal Pharmaceuticals LLC. The label states it is sterile and non-pyrogenic, for intravenous use only, with 10 vials of 2 mL each. Includes storage instructions and manufacturer information for Amneal Pharmaceuticals Pvt. Ltd. and distribution details for Amneal Pharmaceuticals LLC.*

FDA Label Image

8 (Paricalcitol Injection 8)

Label for Paricalcitol Injection, USP 10 mcg/2 mL (5 mcg/mL) intravenous multi-dose vial. Contains paricalcitol 5 mcg per mL with propylene glycol 30% (v/v) and alcohol 20% (v/v). Made in India and distributed by Amneal Pharmaceuticals LLC, Bridgewater, NJ. Includes NDC 70121-1036-1 and space for lot and expiration dates.*

FDA Label Image

9 (Paricalcitol Injection 9)

Paricalcitol Injection, USP 10 mcg/2 mL (5 mcg/mL) multi-dose vials label by Amneal Pharmaceuticals LLC. The sterile, non-pyrogenic intravenous injection is packaged as 10 vials each containing 2 mL. The label notes the vial contents, usage instructions for intravenous use, and storage conditions. Manufactured by Amneal Pharmaceuticals Pvt. Ltd., India, and distributed by Amneal Pharmaceuticals LLC, New Jersey.*

* 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.