Register entry
- Registered sites
- 1
- Active NDC listings
- 0
- Live patents
- 0
- Countries
- 1
- Base
- India
Sites
Registered establishments
1| Establishment | Address | Registered for | FEI / DUNS |
|---|---|---|---|
| KIIOR PHARMA PRIVATE LIMITED | A/10 44/alok/v Nr Arpan, School Nirant Char Rasta, Vastral, Daskroi, Ahmedabad, Gujarat 382418, India (IND) | Active ingredient (API) manufacture | 3043564365771725224 |
Neighbours
Registered in the same town
12- Zydus Lifesciences LimitedAhmedabad, IND · 7 sites
- Amneal Pharmaceuticals of New York, LLCAhmedabad, IND · 6 sites
- Intas Pharmaceuticals LimitedAhmedabad, IND · 3 sites
- Concord Biotech LimitedAhmedabad, IND · 2 sites
- DISHMAN CARBOGEN AMCIS LIMITEDAhmedabad, IND · 2 sites
- Baxter Healthcare CorporationAhmedabad, IND
- Piramal Healthcare (Canada) LimitedAhmedabad, IND
- Hospira, Inc.Ahmedabad, IND
- Emcure Pharmaceuticals LimitedAhmedabad, IND
- Cadila Pharmaceuticals LimitedAhmedabad, IND
- Unimark Remedies LimitedAHMEDABAD, IND
- ALMON HEALTHCARE PRIVATE LIMITEDAHMEDABAD, IND
Compare
Comparable companies in India
- NURAY CHEMICALS PRIVATE LIMITED1 site · 105 NDC
- Jubilant Biosys Limited1 site · 94 NDC
- Maithri Drugs Private Limited1 site · 80 NDC
- MSN Pharmachem Private Limited1 site · 54 NDC
- STHREE CHEMICALS PRIVATE LIMITED1 site · 52 NDC
- Dasami Lab Private Limited1 site · 48 NDC
- AZICO BIOPHORE INDIA PRIVATE LIMITED1 site · 43 NDC
- APOTHECON PHARMACEUTICALS PRIVATE LIMITED1 site · 38 NDC
- Biophore India Pharmaceuticals Private Limited1 site · 38 NDC
- Aurore Pharmaceuticals Private Limited1 site · 33 NDC
Enquiry
Common questions
- Is KIIOR PHARMA PRIVATE LIMITED FDA approved?
- KIIOR PHARMA PRIVATE LIMITED holds 1 FDA-registered establishment 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 KIIOR PHARMA PRIVATE LIMITED's drugs manufactured?
- The FDA register lists Ahmedabad. Registered operations: active ingredient (API) 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.