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Data / Drug companies / Vijayasri Organics Private Limited

Vijayasri Organics Private Limited: 11 products in the FDA NDC directory, labeler code 70159

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

Vijayasri Organics Private Limited (labeler code 70159) lists 11 products in the FDA National Drug Code Directory. By type: 11 bulk ingredients. Its main marketing category is bulk ingredients. The newest product started marketing on December 31, 2022.

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Labeler code
70159
Products in commercial distribution
11
Packages
11
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
February 2, 2016
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Bulk ingredients872.7%
Bulk ingredients for compounding327.3%

Products by type

TypeProductsShare
Bulk ingredients11100%

Dosage forms

Dosage formProductsShare
Powder11100%

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Hydroxyzine hydrochloride70159-008PowderBulk ingredientsDecember 31, 2022
Hydroxyzine hydrochloride70159-008PowderBulk ingredientsDecember 31, 2022
Hydroxyzine hydrochloride70159-008PowderBulk ingredientsDecember 31, 2022
Hydroxyzine hydrochloride70159-008PowderBulk ingredientsDecember 31, 2022
Hydroxyzine hydrochloride70159-008PowderBulk ingredientsDecember 31, 2022
Hydroxyzine hydrochloride70159-008PowderBulk ingredientsDecember 28, 2022
Terbinafine hydrochloride70159-006PowderBulk ingredientsSeptember 12, 2017
Penicillamine70159-004PowderBulk ingredientsSeptember 12, 2017
Zidovudine70159-003PowderBulk ingredients for compoundingFebruary 2, 2016
Nevirapine70159-002PowderBulk ingredients for compoundingFebruary 2, 2016
Lamivudine70159-001PowderBulk ingredients for compoundingFebruary 2, 2016

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.