Product Images Leuprolide Acetate

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Product Label Images

The following 17 images provide visual information about the product associated with Leuprolide Acetate NDC 47335-936 by Sun Pharmaceutical Industries, Inc., such as packaging, labeling, and the appearance of the drug itself. This resource could be helpful for medical professionals, pharmacists, and patients seeking to verify medication information and ensure they have the correct product.

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leuprolide-fig-1 - leuprolide fig 1

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leuprolide-innercarton - leuprolide innercarton

Leuprolide Acetate Injection is a medication given by subcutaneous injection. The medication comes in a 2.8 mL multiple-dose sterile injection vial and contains 14 mg/2.8 mL, which is equivalent to 1 mg/0.2 mL. Each 2 mL of the medication contains euprolide acetate 1 mg (freebase 0.95 mg), sodium chloride, and benzyl alcohol as a preservative. The medication also makes use of other agents such as water, sulfuric acid and hydrochloric acid. This medication is only available on prescription and should be handled with care.*

leuprolide-label - leuprolide label

leuprolide-label - leuprolide label

This is a medication called Leuprolide Acetate. The package insert contains information on dosages. It must be stored at a temperature between 20° to 25°C (68°to 77°F), with excursions permitted to 15° to 30°C (59° to 86°F) which should not be exceeded. It is a 2.8 mL multiple-dose sterile injection vial. Protect it from light, and it is for subcutaneous injection only. It must be stored in the carton until use, and should be kept out of the reach of children. It is sold by Sun Pharmaceutical Ind., Inc., Cranbury, NJ 08512 and manufactured by Sun Pharmaceutical Ind. Ltd., India. The batch number is PJLB2394A ISS. 08/2015.*

leuprolide-outercarton - leuprolide outercarton

leuprolide-outercarton - leuprolide outercarton

This is a medication called Leuprolide Acetate Injection with a strength of 14 mg/2.8 mL (1 mg/0.2 mL), intended for subcutaneous injection. It comes in a kit with enough medication for a 14-day patient administration. A prescription is required to obtain it. A dispensing instruction is included stating that the prescription label should remain with the kit during use. The manufacturer may be SUN PHARMA. The National Drug Code (NDC) for this medication is 47335-936-40.*

leuprolide-structure - leuprolide structure

leuprolide-structure - leuprolide structure

* The product label images have been analyzed using a combination of traditional computing and machine learning techniques. It should be noted that the descriptions provided may not be entirely accurate as they are experimental in nature. Use the information in this page at your own discretion and risk.