Is Andhra Organics Limited FDA approved?

Andhra Organics 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 Andhra Organics Limited's drugs manufactured?

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

What drugs does Andhra Organics Limited make?

2 products are listed under Andhra Organics 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.

Andhra Organics Limited

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

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Registered sites: 1
Active NDC listings: 2
Live patents: 0
Countries: 1
Base: India

Sites

Registered establishments

Establishment	Address	Registered for	FEI / DUNS
Andhra Organics Limited	Plot No 110A, I.D.A., Pydibhimavaram (V), Ranasthalam (M), Srikakulam District, Andhra Pradesh 532409, India (IND)	Active ingredient (API) manufacture	3008430469725026384

Catalogue

Drug listings by form and route

2 active NDC listings: 2 bulk ingredient. By marketing category: BULK INGREDIENT 2.

Dosage form	NDCs
powder	2

Route	NDCs

Labeller name on the listing	NDCs
andhra organics limited	2

Catalogue

Marketed products

Brand	Generic name	Form / route	NDC
-	Sulfadiazine	powder	72672-003BULK INGREDIENT
-	Trimethoprim	powder	72672-001BULK INGREDIENT

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Common questions

Is Andhra Organics Limited FDA approved?: Andhra Organics 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 Andhra Organics Limited's drugs manufactured?: The FDA register lists Srikakulam District. Registered operations: active ingredient (API) manufacture.
What drugs does Andhra Organics Limited make?: 2 products are listed under Andhra Organics 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.