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Data / Drug companies / Zydus Lifesciences Limited

Zydus Lifesciences Limited: 5 products in the FDA NDC directory, labeler code 49315

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

Zydus Lifesciences Limited (labeler code 49315) lists 5 products in the FDA National Drug Code Directory, covering 3 finished drugs by generic name. By type: 5 prescription drugs. Its main marketing category is generic drugs (ANDA). The newest product started marketing on September 14, 2020.

The request: Watch Zydus Lifesciences Limited (FDA labeler code 49315): each new product listing and each discontinued product. $10 of work on sign-up, no card.

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Labeler code
49315
Products in commercial distribution
5
Packages
5
Finished drugs by generic name
3
Prescription products
5
Over the counter products
0
Flagged as original packager
5 of 5 products that carry the flag
Started marketing in the last 12 months
0
Earliest marketing start
May 10, 2017
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Generic drugs (ANDA)5100%

Products by type

TypeProductsShare
Prescription drugs5100%

Drugs it lists

Finished drugs by generic name, with how many companies list each.

DrugProductsCompanies listing it
Doxorubicin hydrochloride220
Arsenic trioxide221
Clofarabine19

Dosage forms

Dosage formProductsShare
Injectable, liposomal240%
Injection, solution240%
Injection120%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Doxorubicin hydrochloride49315-009Injectable, liposomalGeneric drugs (ANDA)September 14, 2020
Doxorubicin hydrochloride49315-008Injectable, liposomalGeneric drugs (ANDA)September 14, 2020
Arsenic trioxide49315-007Injection, solutionGeneric drugs (ANDA)September 3, 2019
Arsenic trioxide49315-005Injection, solutionGeneric drugs (ANDA)November 14, 2018
Clofarabine49315-003InjectionGeneric drugs (ANDA)May 10, 2017

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.