Suppliers / Tablets India

Tablets India

India 2 duplicate records merged Updated 9 July 2026

Tablets India is a finished-dose manufacturer based in India. It appears in 169 regulatory filings across 7 regulators, without an active US DMF or CEP on file. Its filings concentrate with DIGEMAPS (DO), NCELS (KZ) and DAV (Vietnam). Its GMP standing is certified by CDSCO (India) and NAFDAC (NG). Customs aggregates show $3.4M of exports covering 474 molecules to 2 destinations in 2025.

0
active US DMFs
0
valid CEPs
2
registered plants
169
filings across 7 regulators

Registered plants

Site FDA FEI
Chennai, India Not on file
liquid injection and dry injection, India Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
DIGEMAPS (DO) 145 None
NCELS (KZ) 6 None
DAV (Vietnam) 6 None
UZPHARM (UZ) 5 None
FDA (GH) 3 None
NAFDAC (NG) 2 1
CDSCO (India) None 70

Scale

Year Revenue Exports Destinations
2026 YTD Not reported $607K 2
2025 Not reported $3.4M 2
2024 Not reported $3.2M 2
2023 Not reported $3.4M 2

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 We do not publish the identity of any buyer.

Questions about Tablets India

Does Tablets India hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Tablets India. It does have 169 filings with 7 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Tablets India manufacture?
2 registered sites are on record, in India (Chennai and Liquid Injection And Dry Injection). Every site is listed on this page with the register it came from.
Which regulators recognise Tablets India's GMP?
Current GMP certificates are on record from CDSCO (India) and NAFDAC (NG). 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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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