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Data / Drug companies / Virupaksha Organics Limited

Virupaksha Organics Limited: 13 products in the FDA NDC directory, labeler code 51686

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

Virupaksha Organics Limited (labeler code 51686) lists 13 products in the FDA National Drug Code Directory. By type: 13 bulk ingredients. Its main marketing category is bulk ingredients. The newest product started marketing on December 27, 2025.

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Labeler code
51686
Products in commercial distribution
13
Packages
13
Finished drugs by generic name
0
Prescription products
0
Over the counter products
0
Controlled substance products
Schedule IV 1
Started marketing in the last 12 months
1
Earliest marketing start
June 19, 2004
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Bulk ingredients1292.3%
Bulk ingredients for compounding17.7%

Products by type

TypeProductsShare
Bulk ingredients13100%

Dosage forms

Dosage formProductsShare
Powder13100%

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Ranolazine51686-0015PowderBulk ingredientsDecember 27, 2025
Dextromethorphan hydrobromide51686-0014PowderBulk ingredientsDecember 3, 2024
Bilastine51686-0013PowderBulk ingredientsDecember 3, 2024
Citalopram hydrobromide51686-0007PowderBulk ingredientsJanuary 3, 2024
Crisaborole51686-0005PowderBulk ingredientsNovember 11, 2022
Escitalopram oxalate51686-0011PowderBulk ingredientsJanuary 13, 2022
Capsaicin51686-0003PowderBulk ingredientsNovember 16, 2010
Capsaicin51686-0002PowderBulk ingredientsNovember 16, 2010
Efinaconazole51686-0012PowderBulk ingredientsOctober 16, 2007
Fluconazole51686-0006PowderBulk ingredientsOctober 16, 2007
Flurbiprofen51686-0004PowderBulk ingredientsOctober 16, 2007
Fexofenadine hydrochloride51686-0001PowderBulk ingredientsOctober 16, 2007
Tramadol hcl51686-0009PowderBulk ingredients for compoundingJune 19, 2004

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.