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Data / Drug companies / Swati Spentose Private Limited

Swati Spentose Private Limited: 16 products in the FDA NDC directory, labeler code 52119

Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).

Swati Spentose Private Limited (labeler code 52119) lists 16 products in the FDA National Drug Code Directory. By type: 16 bulk ingredients. Its main marketing category is bulk ingredients. The newest product started marketing on July 1, 2025.

The request: Watch Swati Spentose Private Limited (FDA labeler code 52119): each new product listing and each discontinued product. $10 of work on sign-up, no card.

SpecStream is the live web data engine for teams and agents. It reads the National Drug Code Directory that FDA publishes, and this page is that reading. Ask for the companies that make a drug, a class or a dosage form, with their headquarters, website and size added from the web, and new listings and discontinued products arrive in your sheet, CRM, Slack or agent as FDA posts them.

Labeler code
52119
Products in commercial distribution
16
Packages
97
Finished drugs by generic name
0
Prescription products
0
Over the counter products
0
Started marketing in the last 12 months
0
Earliest marketing start
August 20, 2012
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Bulk ingredients16100%

Products by type

TypeProductsShare
Bulk ingredients16100%

Dosage forms

Dosage formProductsShare
Powder16100%

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Silodosin52119-025PowderBulk ingredientsJuly 1, 2025
Tamsulosin hydrochloride52119-024PowderBulk ingredientsJanuary 5, 2024
Prilocaine52119-020PowderBulk ingredientsMarch 20, 2023
Pentosan polysulfate sodium52119-023PowderBulk ingredientsJanuary 10, 2023
Melatonin52119-017PowderBulk ingredientsJuly 1, 2019
Prilocaine hydrochloride52119-016PowderBulk ingredientsJuly 1, 2019
Meloxicam52119-003PowderBulk ingredientsFebruary 7, 2019
Diphenhydramine hydrochloride52119-013PowderBulk ingredientsMay 30, 2016
Diphenhydramine52119-012PowderBulk ingredientsMay 30, 2016
Lidocaine hydrochloride52119-009PowderBulk ingredientsMarch 20, 2014
Lidocaine52119-008PowderBulk ingredientsMarch 20, 2014
Phenytoin52119-007PowderBulk ingredientsAugust 20, 2012
Phenytoin sodium52119-006PowderBulk ingredientsAugust 20, 2012
Pentosan polysulfate sodium52119-005PowderBulk ingredientsAugust 20, 2012
Lidocaine hydrochloride52119-002PowderBulk ingredientsAugust 20, 2012
Lidocaine52119-001PowderBulk ingredientsAugust 20, 2012

CC0 1.0 public domain dedication (openFDA). Counts are products in the FDA National Drug Code Directory on November 6, 2026: 138,262 products in commercial distribution, meaning without a marketing end date in the past. A company is a labeler code; one company can hold several codes, and the directory carries no address. Inclusion in the directory is not FDA approval, and the marketing category says under which kind of application or rule a product is sold. This page uses openFDA data and is not endorsed or certified by FDA. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.