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Data / Drug companies / Maithri Laboratories Private Limited

Maithri Laboratories Private Limited: 24 products in the FDA NDC directory, labeler code 71666

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

Maithri Laboratories Private Limited (labeler code 71666) 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 March 29, 2026.

The request: Watch Maithri Laboratories Private Limited (FDA labeler code 71666): each new product listing and each discontinued product. $10 of work on sign-up, no card.

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Labeler code
71666
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 2, Schedule V 1
Started marketing in the last 12 months
6
Earliest marketing start
August 28, 2017
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
Powder24100%

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Apixaban71666-025PowderBulk ingredientsMarch 29, 2026
Elafibranor71666-024PowderBulk ingredientsMarch 29, 2026
Rebamipide71666-021PowderBulk ingredientsMarch 29, 2026
Suvorexant71666-023PowderBulk ingredientsMarch 28, 2026
Daridorexant hydrochloride71666-020PowderBulk ingredientsMarch 28, 2026
Rabeprazole sodium71666-022PowderBulk ingredientsMarch 27, 2026
Betahistine hydrochloride71666-018PowderBulk ingredientsMarch 29, 2025
Gepirone hydrochloride71666-019PowderBulk ingredientsMarch 25, 2025
Escitalopram oxalate71666-017PowderBulk ingredientsMarch 20, 2025
Lumateperone tosylate71666-016PowderBulk ingredientsSeptember 20, 2023
Viloxazine hydrochloride71666-015PowderBulk ingredientsAugust 25, 2023
Buspirone hydrochloride71666-013PowderBulk ingredientsMarch 28, 2023
Salcaprozate sodium71666-012PowderBulk ingredientsMarch 19, 2021
Pyridostigmine bromide71666-011PowderBulk ingredientsAugust 14, 2020
Cysteamine bitartrate71666-010PowderBulk ingredientsApril 24, 2020
Tolterodine tartrate71666-009PowderBulk ingredientsMarch 28, 2020
Valganciclovir hydrochloride71666-008PowderBulk ingredientsFebruary 28, 2020
Brivaracetam71666-007PowderBulk ingredientsMarch 29, 2019
Chlorpromazine hydrochloride71666-006PowderBulk ingredientsNovember 29, 2018
Ivabradine hydrochloride71666-003PowderBulk ingredientsOctober 22, 2018
Fesoterodine fumarate71666-005PowderBulk ingredientsSeptember 29, 2018
Eliglustat tartrate (premix)71666-002PowderBulk ingredientsMarch 28, 2018
Eliglustat tartrate71666-004PowderBulk ingredientsMarch 27, 2018
Flucytosine71666-001PowderBulk ingredientsAugust 28, 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.