Ciclopirox
- Product NDC
- 68788-7138
- 11-digit product format
- 687887138
- Labeler code
- 68788
- Product ID
- 68788-7138_bdd6225b-935f-4cd2-8ccb-6121ec872f0f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ciclopirox
- Dosage form
- SOLUTION
- Route
- TOPICAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA078270
- Marketing category
- ANDA
- Marketing start
- 2018-04-10
- Marketing end
- 0000-00-00
- Substance
- CICLOPIROX
- Active strength
- 71 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
- 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 |
|---|
| 68788-7138-6 | 68788713806 | 1 BOTTLE in 1 CARTON (68788-7138-6) > 6.6 mL in 1 BOTTLE | 1 bottle | 2018-04-10 | 0000-00-00 | No | No | Current |