Suppliers / Reliance Formulation Pvt. Ltd. 7/2-A

Reliance Formulation Pvt. Ltd. 7/2-A

India Updated 9 July 2026

Reliance Formulation Pvt. Ltd. 7/2-A is a finished-dose manufacturer based in India. It appears in 39 regulatory filings across 1 regulator, without an active US DMF or CEP on file. Its GMP standing is certified by CDSCO (India).

0
active US DMFs
0
valid CEPs
2
registered plants
39
filings across 1 regulators

Registered plants

Site FDA FEI
vatvaahmedabad 382 445 ahmedabad, India Not on file
Ahmedabad, India Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
DIGEMAPS (DO) 39 None
CDSCO (India) None 4

Questions about Reliance Formulation Pvt. Ltd. 7/2-A

Does Reliance Formulation Pvt. Ltd. 7/2-A hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Reliance Formulation Pvt. Ltd. 7/2-A. It does have 39 filings with one regulator, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Reliance Formulation Pvt. Ltd. 7/2-A manufacture?
2 registered sites are on record, in India (Vatvaahmedabad 382 445 Ahmedabad and Ahmedabad). Every site is listed on this page with the register it came from.
Which regulators recognise Reliance Formulation Pvt. Ltd. 7/2-A's GMP?
Current GMP certificates are on record from CDSCO (India). 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