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Data / Drug companies / Vovantis Laboratories Private Limited

Vovantis Laboratories Private Limited: 24 products in the FDA NDC directory, labeler code 51114

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

Vovantis Laboratories Private Limited (labeler code 51114) lists 24 products in the FDA National Drug Code Directory. By type: 24 drugs for further processing. Its main marketing category is drugs for further processing. The newest product started marketing on October 1, 2026.

The request: Watch Vovantis Laboratories Private Limited (FDA labeler code 51114): each new product listing and each discontinued product. $10 of work on sign-up, no card.

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Labeler code
51114
Products in commercial distribution
24
Packages
24
Finished drugs by generic name
0
Prescription products
0
Over the counter products
0
Started marketing in the last 12 months
13
Earliest marketing start
March 6, 2014
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Drugs for further processing24100%

Products by type

TypeProductsShare
Drugs for further processing24100%

Dosage forms

Dosage formProductsShare
Granule1458.3%
Tablet, effervescent520.8%
Tablet416.7%
Powder14.2%

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Dextromethorphan hydrobromide, guaifenesin51114-0462TabletDrugs for further processingOctober 1, 2026
Acetaminophen, diphenhydramine hydrochloride51114-0455GranuleDrugs for further processingSeptember 21, 2026
Acetaminophen, diphenhydramine hydrochloride51114-0461GranuleDrugs for further processingJanuary 1, 2026
Acetaminophen, dextromethorphan hydrobromide51114-0460GranuleDrugs for further processingJanuary 1, 2026
Acetaminophen, dextromethorphan hydrobromide, chlorpheniramine maleate51114-0459GranuleDrugs for further processingJanuary 1, 2026
Acetaminophen, dextromethorphan hydrobromide51114-0458GranuleDrugs for further processingJanuary 1, 2026
Acetaminophen, dextromethorphan hydrobromide, chlorpheniramine maleate51114-0457GranuleDrugs for further processingJanuary 1, 2026
Acetaminophen, dextromethorphan hydrobromide51114-0456GranuleDrugs for further processingJanuary 1, 2026
Acetaminophen, dextromethorphan hydrobromide, chlorpheniramine maleate51114-0454GranuleDrugs for further processingJanuary 1, 2026
Acetaminophen, dextromethorphan hydrobromide51114-0453GranuleDrugs for further processingJanuary 1, 2026
Acetaminophen, dextromethorphan hydrobromide, chlorpheniramine maleate51114-0452GranuleDrugs for further processingJanuary 1, 2026
Acetaminophen, dextromethorphan hydrobromide51114-0451GranuleDrugs for further processingJanuary 1, 2026
Acetaminophen, dextromethorphan hydrobromide51114-0450GranuleDrugs for further processingJanuary 1, 2026
Pyrantel pamoate51114-0726TabletDrugs for further processingAugust 29, 2025
Pyrantel pamoate51114-0725TabletDrugs for further processingMay 30, 2025
Pyrantel pamoate51114-0924GranuleDrugs for further processingSeptember 23, 2024
Pyrantel pamoate51114-0724GranuleDrugs for further processingJuly 15, 2024
Sennosides51114-0225TabletDrugs for further processingFebruary 28, 2022
Acetaminophen, chlorpheniramine maleate, dextromethorphan hydrobromide, phenylephrine hydrochloride51114-0222Tablet, effervescentDrugs for further processingMay 15, 2015
Acetaminophen51114-0221Tablet, effervescentDrugs for further processingFebruary 9, 2015
Diphenhydramine hydrochloride51114-0220Tablet, effervescentDrugs for further processingFebruary 9, 2015
Acetaminophen51114-0219Tablet, effervescentDrugs for further processingFebruary 9, 2015
Acetaminophen51114-0218Tablet, effervescentDrugs for further processingFebruary 9, 2015
Psyllium husk51114-0214PowderDrugs for further processingMarch 6, 2014

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.