Is Coral Drugs Private Limited FDA approved?

Coral Drugs 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 Coral Drugs Private Limited's drugs manufactured?

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

What drugs does Coral Drugs Private Limited make?

13 products are listed under Coral Drugs 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.

Coral Drugs Private Limited

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

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Registered sites: 1
Active NDC listings: 13
Live patents: 0
Countries: 1
Base: India

Sites

Registered establishments

Establishment	Address	Registered for	FEI / DUNS
Coral Drugs Private Limited	55-56-57 HSIIDC Industrial Estate Murthal, Sonipat, 131039, India (IND)	Active ingredient (API) manufacture	3003496619650564870

Catalogue

Drug listings by form and route

13 active NDC listings: 13 bulk ingredient. By marketing category: BULK INGREDIENT 13.

Dosage form	NDCs
powder	13

Route	NDCs

Labeller name on the listing	NDCs
coral drugs private limited	13

Catalogue

Marketed products

Brand	Generic name	Form / route	NDC
-	Azelastine Hydrochloride	powder	49076-7601BULK INGREDIENT
-	Budesonide	powder	49076-6111BULK INGREDIENT
-	Danazol	powder	49076-5201BULK INGREDIENT
-	Danazol	powder	49076-5251BULK INGREDIENT
-	Fluticasone Furoate	powder	49076-6451BULK INGREDIENT
-	Fluticasone Furoate	powder	49076-6452BULK INGREDIENT
-	Fluticasone Propionate	powder	49076-5501BULK INGREDIENT
-	Formoterol Fumarate Dihydrate	powder	49076-7001BULK INGREDIENT
-	Isoflupredone Acetate	powder	49076-7301BULK INGREDIENT
-	Mometasone Furoate	powder	49076-5603BULK INGREDIENT
-	Mometasone Furoate Monohydrate	powder	49076-5701BULK INGREDIENT
-	Mometasone Furoate Monohydrate	powder	49076-5702BULK INGREDIENT
-	Triamcinolone Acetonide	powder	49076-6701BULK INGREDIENT

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Enquiry

Common questions

Is Coral Drugs Private Limited FDA approved?: Coral Drugs 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 Coral Drugs Private Limited's drugs manufactured?: The FDA register lists Sonipat. Registered operations: active ingredient (API) manufacture.
What drugs does Coral Drugs Private Limited make?: 13 products are listed under Coral Drugs 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.