Ciclesonide
- Product NDC
- 66993-015
- 11-digit product format
- 669930015
- Labeler code
- 66993
- Product ID
- 66993-015_0f3cfe0c-d7aa-4e7c-9a39-63be94f861ca
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ciclesonide
- Dosage form
- AEROSOL, METERED
- Route
- NASAL
- Labeler
- Prasco Laboratories
- Application
- NDA202129
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2022-04-23
- Marketing end
- 0000-00-00
- Substance
- CICLESONIDE
- Active strength
- 37 ug/1
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 66993-015-64 | 66993001564 | 1 CANISTER in 1 CARTON (66993-015-64) > 60 AEROSOL, METERED in 1 CANISTER | 1 canister | 2022-04-23 | 0000-00-00 | No | No | Current |