Suppliers / Scott-Edil Pharmacia

Scott-Edil Pharmacia

India 321 employees 3 duplicate records merged Updated 9 July 2026

Scott-Edil Pharmacia is a finished-dose manufacturer based in India. It appears in 221 regulatory filings across 7 regulators, without an active US DMF or CEP on file. Its filings concentrate with EFDA (ET), NAFDAC (NG) and ARCSA (EC). Its GMP standing is certified by TMDA (TZ), NAFDAC (NG) and FDA (GH). Customs aggregates show $74.2M of exports covering 3,763 molecules to 51 destinations in 2025.

0
active US DMFs
0
valid CEPs
1
registered plants
221
filings across 7 regulators

Registered plants

Site FDA FEI
Baddi District Solan HP India, Nigeria Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
EFDA (ET) 86 None
NAFDAC (NG) 57 2
ARCSA (EC) 32 None
DIGEMAPS (DO) 22 None
UZPHARM (UZ) 18 None
ZAMRA (ZM) 4 None
TMDA (TZ) None 3
FDA (GH) None 1

Scale

Year Revenue Exports Destinations
2026 YTD Not reported $10.1M 29
2025 Not reported $74.2M 51
2024 Not reported $51.1M 57
2023 Not reported $40.9M 53

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 We do not publish the identity of any buyer.

Questions about Scott-Edil Pharmacia

Does Scott-Edil Pharmacia hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Scott-Edil Pharmacia. It does have 221 filings with 7 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Scott-Edil Pharmacia manufacture?
1 registered site is on record, in Nigeria (Baddi District Solan HP India). Every site is listed on this page with the register it came from.
Which regulators recognise Scott-Edil Pharmacia's GMP?
Current GMP certificates are on record from TMDA (TZ), NAFDAC (NG) and FDA (GH). 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