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Data / Drug companies / Emnar Pharma Private Limited

Emnar Pharma Private Limited: 24 products in the FDA NDC directory, labeler code 71901

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

Emnar Pharma Private Limited (labeler code 71901) lists 24 products in the FDA National Drug Code Directory. By type: 24 bulk ingredients. Its main marketing category is bulk ingredients. The newest product started marketing on August 24, 2025.

The request: Watch Emnar Pharma Private Limited (FDA labeler code 71901): each new product listing and each discontinued product. $10 of work on sign-up, no card.

SpecStream is the live web data engine for teams and agents. It reads the National Drug Code Directory that FDA publishes, and this page is that reading. Ask for the companies that make a drug, a class or a dosage form, with their headquarters, website and size added from the web, and new listings and discontinued products arrive in your sheet, CRM, Slack or agent as FDA posts them.

Labeler code
71901
Products in commercial distribution
24
Packages
24
Finished drugs by generic name
0
Prescription products
0
Over the counter products
0
Controlled substance products
Schedule IV 1, Schedule V 1
Started marketing in the last 12 months
0
Earliest marketing start
January 1, 1987
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Bulk ingredients24100%

Products by type

TypeProductsShare
Bulk ingredients24100%

Dosage forms

Dosage formProductsShare
Powder2291.7%
Injection14.2%
Tablet14.2%

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Lamivudine71901-629PowderBulk ingredientsAugust 24, 2025
Capecitabine71901-628PowderBulk ingredientsAugust 24, 2025
Calcium carbonate71901-626PowderBulk ingredientsAugust 24, 2025
Sodium valproate71901-625PowderBulk ingredientsAugust 24, 2025
Sodium chloride71901-624PowderBulk ingredientsAugust 24, 2025
Empagliflozin (efg)71901-623PowderBulk ingredientsAugust 24, 2025
Potassium bicarbonate71901-622PowderBulk ingredientsAugust 24, 2025
Potassium chloride71901-621PowderBulk ingredientsAugust 24, 2025
Apixaban71901-620PowderBulk ingredientsAugust 23, 2025
Lithium carbonate71901-619PowderBulk ingredientsAugust 23, 2025
Tenofovir disoproxil fumarate71901-618PowderBulk ingredientsAugust 23, 2025
Pridinol mesilate71901-617PowderBulk ingredientsAugust 23, 2025
Bupropion hydrochloride71901-615PowderBulk ingredientsAugust 20, 2025
Pitolisant hydrochloride71901-614PowderBulk ingredientsMarch 19, 2025
Zonisamide71901-613PowderBulk ingredientsMarch 18, 2025
Lacosamide71901-611PowderBulk ingredientsDecember 27, 2023
Gabapentin71901-609PowderBulk ingredientsApril 19, 2022
Empagliflozin71901-608PowderBulk ingredientsFebruary 17, 2022
Dapagliflozin propanediol monohydrate71901-607PowderBulk ingredientsNovember 12, 2021
Levetiracetam71901-605PowderBulk ingredientsDecember 7, 2020
Acotiamide hydrochloride hydrate71901-603TabletBulk ingredientsJanuary 31, 2018
Tramadol hydrochloride71901-601PowderBulk ingredientsJanuary 31, 2018
Sodium bicarbonate71901-604InjectionBulk ingredientsDecember 1, 2017
Ciprofloxacin hydrochloride71901-602PowderBulk ingredientsJanuary 1, 1987

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.