Ciclesonide
- Product NDC
- 66993-572
- 11-digit product format
- 669930572
- Labeler code
- 66993
- Product ID
- 66993-572_38807433-3368-4133-aed1-321f1fa62fdc
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ciclesonide
- Dosage form
- AEROSOL, METERED
- Route
- RESPIRATORY (INHALATION)
- Labeler
- Prasco Laboratories
- Application
- NDA021658
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2021-05-01
- Marketing end
- 0000-00-00
- Substance
- CICLESONIDE
- Active strength
- 160 ug/1
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 66993-572-64 | 66993057264 | 1 INHALER in 1 CARTON (66993-572-64) > 60 AEROSOL, METERED in 1 INHALER | 1 inhaler | 2021-05-01 | 0000-00-00 | No | No | Current |