Is SYNTHIMED LABS PRIVATE LIMITED FDA approved?

SYNTHIMED LABS PRIVATE LIMITED holds 1 FDA-registered establishment in India. Registration puts a site on the FDA's register and open to inspection; it is not an approval of the company. Approvals attach to individual drug applications.

Where are SYNTHIMED LABS PRIVATE LIMITED's drugs manufactured?

The FDA register lists Mohali. Registered operations: active ingredient (API) manufacture.

What drugs does SYNTHIMED LABS PRIVATE LIMITED make?

14 products are listed under SYNTHIMED LABS PRIVATE LIMITED in the openFDA NDC Directory, most often as powder. The full breakdown by dosage form and route is above. A listing count is not a sales figure.

SYNTHIMED LABS PRIVATE LIMITED

Data as of 24 Sept 2026 · How to read this entry

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Registered sites: 1
Active NDC listings: 14
Live patents: 0
Countries: 1
Base: India

Sites

Registered establishments

Establishment	Address	Registered for	FEI / DUNS
SYNTHIMED LABS PRIVATE LIMITED	Village Bhagwanpura, Barwala Road, Derabassi, Mohali, Punjab 140507, India (IND)	Active ingredient (API) manufacture	3005895238918604344

Catalogue

Drug listings by form and route

14 active NDC listings: 14 bulk ingredient. By marketing category: BULK INGREDIENT 14.

Dosage form	NDCs
powder	14

Route	NDCs

Labeller name on the listing	NDCs
synthimed labs private limited	14

Catalogue

Marketed products

Brand	Generic name	Form / route	NDC
-	Acamprosate Calcium	powder	65096-0112BULK INGREDIENT
-	Anastrozole	powder	65096-0117BULK INGREDIENT
-	Aripiprazole	powder	65096-0107BULK INGREDIENT
-	Cinacalcet Hydrochloride	powder	65096-0114BULK INGREDIENT
-	Clarithromycin	powder	65096-0100BULK INGREDIENT
-	Donepezil Hydrochloride	powder	65096-0109BULK INGREDIENT
-	Ezetimibe	powder	65096-0113BULK INGREDIENT
-	Pioglitazone Hydrochloride	powder	65096-0104BULK INGREDIENT
-	Quetiapine Fumarate	powder	65096-0106BULK INGREDIENT
-	Risedronate Sodium	powder	65096-0110BULK INGREDIENT
-	Ropinirole Hydrochloride	powder	65096-0102BULK INGREDIENT
-	fexofenadine hydrochloride	powder	65096-0103BULK INGREDIENT
-	letrozole	powder	65096-0116BULK INGREDIENT
-	nateglinide	powder	65096-0108BULK INGREDIENT

Neighbours

Registered in the same town

Sun Pharmaceutical Industries LimitedMohali, IND

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Enquiry

Common questions

Is SYNTHIMED LABS PRIVATE LIMITED FDA approved?: SYNTHIMED LABS PRIVATE LIMITED holds 1 FDA-registered establishment in India. Registration puts a site on the FDA's register and open to inspection; it is not an approval of the company. Approvals attach to individual drug applications.
Where are SYNTHIMED LABS PRIVATE LIMITED's drugs manufactured?: The FDA register lists Mohali. Registered operations: active ingredient (API) manufacture.
What drugs does SYNTHIMED LABS PRIVATE LIMITED make?: 14 products are listed under SYNTHIMED LABS PRIVATE LIMITED in the openFDA NDC Directory, most often as powder. The full breakdown by dosage form and route is above. A listing count is not a sales figure.

Compiled from FDA establishment registrations, the openFDA NDC Directory, the Orange Book and the FDA drug shortage database. Not claimed by the company. Sources and methodology.