Heparin Sodium Injection, Solution
Product Images NDC 63739-931

Product Visual Gallery

This gallery contains 19 technical images submitted to the FDA as part of the official labeling for Heparin Sodium (NDC 63739-931). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Mckesson Corporation Dba Sky Packaging, 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

Package Label-principal Display Panel (1,000 USP Units/mL)

Heparin Sodium Injection, USP 1,000 USP Units/mL multiple dose vial label. The label includes NDC 63739-920-11 and states the product is for intravenous or subcutaneous use in a 1 mL vial. It notes the drug is derived from porcine intestinal mucosa, sterile, and nonpyrogenic, with storage instructions between 20° to 25°C. Manufactured in India for McKesson Corporation dba SKY Packaging. A barcode and a QR code are also visible.*

FDA Label Image

Package Label-principal Display Panel (10,000 USP Units/mL)

Packaging label for Heparin Sodium Injection, USP 10,000 USP units/mL by McKesson Corporation dba SKY Packaging. The label indicates a 1 mL vial size with 25 multiple dose vials per package. It is intended for intravenous or subcutaneous use, derived from porcine intestinal mucosa, with warnings including "Not for lock flush." The label includes manufacturer and distributor information, storage instructions, and inactive ingredients details.*

FDA Label Image

Package Label-principal Display Panel (50,000 USP Units/5 mL (10,000 USP Units/mL))

Heparin Sodium Injection USP label showing a strength of 50,000 USP Units per 5 mL (10,000 USP Units per mL) in a 5 mL multiple dose vial. The label states use for intravenous or subcutaneous administration, manufactured in India for McKesson Corporation dba SKY Packaging. It specifies storage at 20° to 25°C and notes that the product is derived from porcine intestinal mucosa.*

FDA Label Image

Kage Label-principal Display Panel (50,000 USP Units/5 mL (10,000 USP Units/mL))

Heparin Sodium Injection, USP labeled at 50,000 USP Units per 5 mL (10,000 USP Units/mL) in a 5 mL multiple dose vial. The label states it is for intravenous or subcutaneous use and derived from porcine intestinal mucosa. It carries a warning "Not For Lock Flush". Manufactured by Aurobindo Pharma Limited and distributed by McKesson Corporation dba SKY Packaging.*

FDA Label Image

Package Label-principal Display Panel (20,000 USP Units/mL)

Label of Heparin Sodium Injection USP, 20,000 USP Units/mL, a multiple dose vial for intravenous or subcutaneous use. The label includes storage instructions at 20° to 25°C, states the product is sterile and nonpyrogenic, and notes it is derived from porcine intestinal mucosa. Manufactured in India for McKesson Corporation dba SKY Packaging, the label also indicates it is not for lock flush use.*

FDA Label Image

Package Label-principal Display Panel (20,000 USP Units/mL)

Packaging label for Heparin Sodium Injection, USP 20,000 USP Units/mL by McKesson Corporation dba SKY Packaging. The label indicates the product is a 1 mL solution in 25 multiple dose vials derived from porcine intestinal mucosa for intravenous or subcutaneous use. The label includes warnings such as "NOT FOR LOCK FLUSH" and storage instructions. Manufactured by Aurobindo Pharma Limited, India.*

FDA Label Image

Heparin Fig15

Label for Heparin Sodium Injection, USP 2,000 USP Units per 2 mL (1,000 USP Units per mL) single dose vial. The injectable solution is preservative-free for intravenous or subcutaneous use. It is derived from porcine intestinal mucosa, sterile, and nonpyrogenic. The product is stored at 20° to 25°C (68° to 77°F) and manufactured in India for McKesson Corporation dba SKY Packaging. The label includes an NDC code 63739-900-12 and a barcode.*

FDA Label Image

Heparin Fig16

Heparin Sodium 2,000 USP Units/2 mL (1,000 USP Units/mL) injection solution carton from McKesson Corporation dba SKY Packaging. The label indicates sterile, preservative-free product for intravenous or subcutaneous use in 25 single dose vials. Manufactured by Aurobindo Pharma Limited, India. Includes storage and usage instructions.*

FDA Label Image

Heparin Fig17

Heparin Sodium Injection, USP label showing 50,000 USP Units/10 mL (5,000 USP Units/mL) strength in a 10 mL multiple dose vial. The label indicates usage for intravenous or subcutaneous injection and contains a warning about benzyl alcohol. Manufactured in India for McKesson Corporation dba SKY Packaging.*

FDA Label Image

Heparin Fig18

Packaging label for Heparin Sodium Injection, USP, 50,000 USP Units per 10 mL (5,000 USP Units/mL) by McKesson Corporation dba SKY Packaging. The label notes the drug is for intravenous or subcutaneous use, available in 25 multiple dose vials, and contains benzyl alcohol. The label includes storage instructions, manufacturer details (Aurobindo Pharma Limited, India), and cautions such as 'NOT FOR LOCK FLUSH.'*

FDA Label Image

Package Label-principal Display Panel (1,000 USP Units/mL)

Packaging label for Heparin Sodium Injection, USP 1,000 USP Units/mL, solution for intravenous or subcutaneous use. The label indicates the product comes in 25 multiple dose vials of 1 mL each, derived from porcine intestinal mucosa. It is distributed by McKesson Corporation dba SKY Packaging and manufactured by Aurobindo Pharma Limited in India. The label features instructions such as "Not for lock flush" and includes storage info and concentration details.*

FDA Label Image

Package Label-principal Display Panel (10,000 USP Units/10 mL (1,000 USP Units/mL))

Heparin Sodium Injection USP label for 10,000 USP Units per 10 mL (1,000 USP Units/mL) multiple dose vial by McKesson Corporation dba SKY Packaging. The label indicates intravenous or subcutaneous use and clearly states it is not for lock flush. Storage instructions specify 20° to 25°C (68° to 77°F). The product is sterile, nonpyrogenic, derived from porcine intestinal mucosa, and manufactured in India.*

FDA Label Image

Package Label-principal Display Panel (10,000 USP Units/10 mL (1,000 USP Units/mL))

Packaging label for Heparin Sodium Injection, USP 10,000 USP Units/10 mL (1,000 USP Units/mL) multiple dose vials, by McKesson Corporation dba SKY Packaging. The label includes warnings 'NOT FOR LOCK FLUSH' and states the product is derived from porcine intestinal mucosa. The volume is 10 mL per vial, for intravenous or subcutaneous use.*

FDA Label Image

Package Label-principal Display Panel (30,000 USP Units/30 mL (1,000 USP Units/mL))

Label of Heparin Sodium Injection, USP, 1,000 USP Units/mL strength, packaged as 30 mL multiple dose vial. The label shows dosing information as 30,000 USP Units per 30 mL, suitable for intravenous or subcutaneous use. Manufactured in India for McKesson Corporation dba SKY Packaging, the label includes storage instructions to keep at 20° to 25°C (68° to 77°F). It states the drug is sterile, derived from porcine intestinal mucosa, and nonpyrogenic.*

FDA Label Image

Package Label-principal Display Panel (30,000 USP Units/30 mL (1,000 USP Units/mL))

Heparin Sodium Injection, USP 30,000 USP Units/30 mL (1,000 USP Units/mL) multiple dose vials. This label from McKesson Corporation dba SKY Packaging details a 30 mL vial derived from porcine intestinal mucosa for intravenous or subcutaneous use. It includes warnings such as NOT FOR LOCK FLUSH and storage instructions, with manufacturer information for Aurobindo Pharma Limited.*

FDA Label Image

Package Label-principal Display Panel (5,000 USP Units/mL)

Heparin Sodium Injection, USP label for 5,000 USP Units/mL strength in a 1 mL multiple dose vial. It is for intravenous (IV) or subcutaneous (SC) use. The label includes storage instructions, manufacturer McKesson Corporation dba SKY Packaging, and indicates the product is sterile and nonpyrogenic, derived from porcine intestinal mucosa. The label clearly states "NOT FOR LOCK FLUSH."*

FDA Label Image

Package Label-principal Display Panel (5,000 USP Units/mL)

Heparin Sodium Injection, USP 5,000 USP Units/mL solution packaging label. The 1 mL vial box is labeled for intravenous or subcutaneous use, containing 25 multiple dose vials. Manufactured by Aurobindo Pharma Limited and distributed by McKesson Corporation dba SKY Packaging. The label highlights that this product is not for lock flush and is derived from porcine intestinal mucosa.*

FDA Label Image

Package Label-principal Display Panel (10,000 USP Units/mL)

Label for Heparin Sodium Injection, USP 10,000 USP Units/mL in a 1 mL multiple dose vial. The label states it is for intravenous or subcutaneous use, derived from porcine intestinal mucosa, sterile and nonpyrogenic. It is manufactured in India for McKesson Corporation dba SKY Packaging, with storage recommended at 20° to 25°C (68° to 77°F). Contains NDC 63739-964-11 and a barcode.*

FDA Label Image

Heparin Chemical Structure (Heparin Str)

Chemical structure diagram of Heparin Sodium, showing five labeled sugar ring components with various functional groups including sulfate and hydroxyl groups, illustrating the molecule's polysaccharide composition.*

* 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.