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ArticlePeer ReviewedOpen AccessPlagiarism Passed
Paper ID:IJSREM52969

Injectable Drug Product Formulation

Stream/Area:

-

Subject:

-

Paper ID:

IJSREM52969

Volume:

9 |

10 |

Oct 2025

Pages:

Publication Frequency:

Monthly (12 issues per year)

DOI
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Not assigned

License:International Journal of Scientific Research in Engineering and Management follows the Creative Commons Attribution 4.0 (CC BY 4.0) License, allowing free use and distribution with proper attribution.

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Authors

NP

Nilesh Prajapati

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Abstract

This study has been undertaken to investigate the Parenteral Formulations are sterile, pyrogen-free, administered by injection through skin layers. This review highlights all the aspects regarding parenteral products advantages, disadvantages, routes of administration, additives, preparation, types of containers and quality control tests for evaluation. They are required, like any pharmaceutical dosage forms, to meet the pharmaceutical quality standards as described in pharma-copeias and to be safe for the intended purpose of use. Sterility can be achieved by different processes of sterilization that should be appropriate to the formulations, while the pyrogen-free aspect will require, if no depyrogenation process is used during the preparation of the sterile drug products, the use of pyrogen-free pharmaceutical ingredients; drug substances or API (Active Pharmaceutical Ingredient) and excipients.

KEYWORDS

Parenteral Formulations Antimicrobial Agents Needle.

Cite This Article

Nilesh Prajapati, "Injectable Drug Product Formulation," International Journal of Scientific Research in Engineering and Management, vol. 9, no. 10, Oct 2025.

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Publication Date

10/29/2025

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Double-Blind Peer Review

Review Rounds: 2

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Conflict of Interest

The authors declare no conflict of interest related to this research work.

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No funding information available for this research.

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