Register entry
Cdymax (India) Pharma Private Limited
Data as of · How to read this entry
- Registered sites
- 2
- Active NDC listings
- 0
- Live patents
- 0
- Countries
- 1
- Base
- India
Authorisation
Registered operations
Active ingredient (API) manufacture1Finished drug manufacture1
Sites
Registered establishments
2| Establishment | Address | Registered for | FEI / DUNS |
|---|---|---|---|
| CDYMAX (INDIA) PHARMA PRIVATE LIMITEDRegistrant: Cdymax (India) Pharma Private Limited | Plot No. 20 and 169, Sy. No. 132, 243 And 244, Rajapura Village Bommasandra Jigani Link Road, Industrial Area, Anekal, Bengalurur 562106, India (IND) | Finished drug manufacture | 3030133758957053589 |
| Cdymax (India) Pharma Private Limited | 77D & 116/117, KIADB Industrial Area Jigani, 2nd Phase, Bengaluru, Karnataka 560105, India (IND) | Active ingredient (API) manufacture | 3009882550916512426 |
Neighbours
Registered in the same town
12- Biocon Biologics LimitedBengaluru, IND · 5 sites
- Micro Labs LimitedBengaluru, IND · 4 sites
- Syngene International LimitedBengaluru, IND · 3 sites
- CIPLA PHARMACEUTICALS LIMITEDBengaluru, IND · 2 sites
- SHILPA MEDICARE LIMITEDBengaluru, IND · 2 sites
- Anthem Biosciences LimitedBengaluru, IND · 2 sites
- ONESOURCE SPECIALTY PHARMA LIMITEDBengaluru, IND · 2 sites
- Eurofins Advinus BioPharma Services India Private LimitedBENGALURU, IND; Bengaluru, IND · 2 sites
- Viatris Inc.Bengaluru, IND
- Apotex Inc.Bengaluru, IND
- Strides Pharma Science LimitedBengaluru, IND
- Eurofins BioPharma Product Testing India Private LimitedBengaluru, IND
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Enquiry
Common questions
- Is Cdymax (India) Pharma Private Limited FDA approved?
- Cdymax (India) Pharma Private Limited holds 2 FDA-registered establishments 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 Cdymax (India) Pharma Private Limited's drugs manufactured?
- The FDA register lists Anekal; Bengaluru. Registered operations: active ingredient (API) manufacture, finished drug manufacture.
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.