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Data / Drug companies / Natco Pharma Limited

Natco Pharma Limited: 53 products in the FDA NDC directory, labeler code 63850

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

Natco Pharma Limited (labeler code 63850) lists 53 products in the FDA National Drug Code Directory, covering 7 finished drugs by generic name. By type: 34 bulk ingredients, 19 prescription drugs. Its main marketing category is bulk ingredients. The newest product started marketing on May 16, 2026.

The request: Watch Natco Pharma Limited (FDA labeler code 63850): each new product listing and each discontinued product. $10 of work on sign-up, no card.

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Labeler code
63850
Products in commercial distribution
53
Packages
71
Finished drugs by generic name
7
Prescription products
19
Over the counter products
0
Flagged as original packager
19 of 19 products that carry the flag
Started marketing in the last 12 months
1
Earliest marketing start
November 23, 2005
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Bulk ingredients3464.2%
Generic drugs (ANDA)1935.8%

Products by type

TypeProductsShare
Bulk ingredients3464.2%
Prescription drugs1935.8%

Drugs it lists

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

DrugProductsCompanies listing it
Everolimus815
Pomalidomide412
Ondansetron tablets21
Trihexyphenidyl hydrochloride28
Letrozole117
Granisetron hydrochloride18
Anastrozole122

Dosage forms

Dosage formProductsShare
Powder3362.3%
Tablet1222.6%
Capsule47.5%
Tablet, film coated35.7%
Injection11.9%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Imatinib63850-8126PowderBulk ingredientsMay 16, 2026
Pomalidomide63850-0134CapsuleGeneric drugs (ANDA)November 1, 2025
Pomalidomide63850-0133CapsuleGeneric drugs (ANDA)November 1, 2025
Pomalidomide63850-0132CapsuleGeneric drugs (ANDA)November 1, 2025
Pomalidomide63850-0131CapsuleGeneric drugs (ANDA)November 1, 2025
Venetoclax63850-8103PowderBulk ingredientsNovember 29, 2023
Acalabrutinib dihydrate63850-8113PowderBulk ingredientsNovember 25, 2023
Idelalisib63850-8098PowderBulk ingredientsNovember 25, 2023
Ruxolitinib phosphate63850-8125PowderBulk ingredientsNovember 24, 2023
Everolimus63850-0061TabletGeneric drugs (ANDA)October 1, 2021
Everolimus63850-0107TabletGeneric drugs (ANDA)May 20, 2021
Everolimus63850-0064TabletGeneric drugs (ANDA)May 20, 2021
Everolimus63850-0063TabletGeneric drugs (ANDA)May 20, 2021
Everolimus63850-0062TabletGeneric drugs (ANDA)May 20, 2021
Nilotinib hydrochloride monohydrate63850-8106PowderBulk ingredientsMay 19, 2021
Lapatinib ditosylate anhydrous63850-7421PowderBulk ingredientsMay 17, 2021
Everolimus63850-0060TabletGeneric drugs (ANDA)March 5, 2021
Everolimus63850-0059TabletGeneric drugs (ANDA)March 5, 2021
Everolimus63850-0058TabletGeneric drugs (ANDA)March 5, 2021
Ibrutinib63850-8089PowderBulk ingredientsJanuary 4, 2020
Gefitinib63850-8070PowderBulk ingredientsJanuary 4, 2020
Sugammadex sodium63850-8099PowderBulk ingredientsJanuary 30, 2019
Chloroquine phosphate63850-8080PowderBulk ingredientsMarch 1, 2018
Teriflunomide63850-8081PowderBulk ingredientsDecember 9, 2017
Glatiramer acetate63850-4035InjectionBulk ingredientsDecember 9, 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.