Suppliers / The Andhra Sugars

The Andhra Sugars

India Updated 9 July 2026

The Andhra Sugars is an API manufacturer based in India. It holds 2 active US drug master files. Its GMP standing is certified by US FDA. Its most recent recorded inspection, by US FDA, closed on 13 September 2024 as NAI. Customs aggregates show $662K of exports covering 32 molecules to 12 destinations in 2025.

2
active US DMFs
0
valid CEPs
1
registered plants 1 with an FDA FEI number
0
filings across 0 regulators
These figures were checked against the regulators' own files on 25 July 2026
Plants
1 of 1 confirmed
Inspections
3 of 3 confirmed
Sources: FDA Establishment Registration, read 4 May 2026. FDA drug inspection classifications, read 4 May 2026.

Inspection history

  • 13 September 2024 NAI US FDA
  • 27 March 2015 VAI US FDA
  • 24 September 2011 VAI US FDA

NAI means no action indicated, VAI means voluntary action indicated, and OAI means official action indicated.

Registered plants

Site FDA FEI
Tanuku, India 3003789475

What they file, and where

Molecule Regulators Docs
Acetylsalicylic Acid US FDA 2

Also appears on these molecule pages

Acetylsalicylic Acid API

Filings and GMP by regulator

Regulator Filings GMP certificates
US FDA None 1

Scale

Year Revenue Exports Destinations
2026 YTD Not reported $10K 3
2025 Not reported $662K 12
2024 Not reported $982K 14
2023 Not reported $526K 14

Export figures are customs aggregates. We do not publish the identity of any buyer.

Questions about The Andhra Sugars

Does The Andhra Sugars hold a US DMF or a CEP?
The Andhra Sugars holds 2 active US drug master files. A drug master file is a submission to the FDA describing how an ingredient is made; a CEP is the EDQM's certificate that the substance meets its European Pharmacopoeia monograph. Both are filings rather than approvals.
Is The Andhra Sugars FDA-registered?
One site operated by The Andhra Sugars carries an FDA establishment identifier (FEI), which means it is registered with the FDA as a drug establishment. Registration is not the same as approval or inspection clearance.
How did The Andhra Sugars's last inspection go?
The most recent inspection on record closed on 13 September 2024 as NAI (No Action Indicated: nothing objectionable was found). 3 inspections are on file.
Where does The Andhra Sugars manufacture?
1 registered site is on record, in India (Tanuku). Every site is listed on this page with the register it came from.
What does The Andhra Sugars make?
1 molecule is on record against The Andhra Sugars, including Acetylsalicylic Acid. Each links through to that molecule's full manufacturer list.
Which regulators recognise The Andhra Sugars's GMP?
Current GMP certificates are on record from US FDA. GMP recognition covers the manufacturing site, separately from any filing on the substance itself.

Answered from this company's own record. Where a register holds nothing, the question is not asked rather than answered with a zero. How we count our figures.

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Open risk flags

  • The most recent inspection outcome was NAI, on 13 September 2024.

Comparable suppliers

Zydus Lifesciences shares 1 molecule Shandong Xinhua Pharmaceutical shares 1 molecule Novacyl SAS shares 1 molecule Hebei Jingye Medical Technology shares 1 molecule JQC (Huayin) Pharmaceutical shares 1 molecule

Ranked by shared active ingredients where we have them, otherwise by country and comparable credentials.

Sources on this page

FDA
Drug master files, establishment registration, inspection classifications
EDQM
Certificates of suitability
EudraGMDP and national regulators
GMP certificates
Customs aggregates
Export values, molecule and destination counts