Omnaris
NDC 70515-701, ciclesonide, spray, from Covis Pharma US, Inc.
- Product NDC
- 70515-701
- Status
- Listed
- Labeler
- Covis Pharma US, Inc
- Dosage form
- SPRAY
- Route
- NASAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- NDA
- Application
- NDA022004
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/70515-701 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- CICLESONIDE50 ug/1
| Package NDC | NDC-11 | Package |
|---|---|---|
| 70515-701-01 | 70515070101 | 1 POUCH in 1 CARTON (70515-701-01) / 1 BOTTLE, GLASS in 1 POUCH / 120 SPRAY in 1 BOTTLE, GLASS |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/15fefd46-ac7e-40d0-b635-e6c3d653c666NADAC price for package 70515070101
GET /v1/drugs/nadac/70515070101
Use it
Look up 70515-701 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/70515-701 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 70515-701. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.