Ciclopirox
- Product NDC
- 0713-0317
- 11-digit product format
- 007130317
- Labeler code
- 0713
- Product ID
- 0713-0317_de0c0ab2-9e23-a0b7-e053-2995a90acdd4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- CICLOPIROX
- Dosage form
- SOLUTION
- Route
- TOPICAL
- Labeler
- Cosette Pharmaceuticals, Inc.
- Application
- ANDA078233
- Marketing category
- ANDA
- Marketing start
- 2007-05-22
- Marketing end
- 2024-06-30
- Substance
- CICLOPIROX
- Active strength
- 80 mg/mL
- Pharmacologic classes
- Decreased DNA Replication [PE], Decreased Protein Synthesis [PE], Decreased RNA Replication [PE], Protein Synthesis Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0713-0317-87 | 00713031787 | 1 BOTTLE, WITH APPLICATOR in 1 CARTON (0713-0317-87) > 3.3 mL in 1 BOTTLE, WITH APPLICATOR | 2007-05-22 | 0000-00-00 | No | No | Current |
| 0713-0317-88 | 00713031788 | 1 BOTTLE, WITH APPLICATOR in 1 CARTON (0713-0317-88) > 6.6 mL in 1 BOTTLE, WITH APPLICATOR | 2007-05-22 | 0000-00-00 | No | No | Current |