Drug
Who makes ciprofloxacin hydrochloride and hydrocortisone?
4 companies list ciprofloxacin hydrochloride and hydrocortisone as a human prescription drug, including under the names CIPRO HC. Forms: suspension/ drops. Routes: auricular (otic).
Labellers from the openFDA NDC Directory. A labeller is the firm named on the label, not necessarily the site that made the product, and a listing is not an FDA approval. Data as of 24 Sept 2026. Methodology
Companies listing ciprofloxacin hydrochloride and hydrocortisone
| Company | Forms | Application | NDCs | Registered sites |
|---|---|---|---|---|
| Sandoz Industrial Products S.AAustria | suspension/ drops | NDA, NDA AUTHORIZED GENERICNDA020805 | 2 | 5 |
| International Medication Systems, Ltd.United States | suspension/ drops | NDANDA020805 | 2 | 3 |
| ASCLEMED USA INC. DBA ENOVACHEMUnited States | suspension/ drops | NDANDA020805 | 1 | 1 |
| Cosette Pharmaceuticals, Inc. | suspension/ drops | ANDAANDA218273 | 1 | 0 |
Enquiry
Common questions
- Who makes ciprofloxacin hydrochloride and hydrocortisone?
- 4 companies list ciprofloxacin hydrochloride and hydrocortisone as a human prescription drug in the openFDA NDC Directory, led by Sandoz Industrial Products S.A, International Medication Systems, Ltd., ASCLEMED USA INC. DBA ENOVACHEM, Cosette Pharmaceuticals, Inc.. Each is the labeller, the firm named on the label; the product may be made at a site registered to another company.
- Is there a generic CIPRO HC?
- 1 company lists ciprofloxacin hydrochloride and hydrocortisone under an abbreviated new drug application (ANDA), the application type used for generics, and 3 under an NDA or BLA. Listing status is from the NDC Directory; it is not a statement of availability.