Ciclopirox Olamine
- Product NDC
- 68071-4162
- 11-digit product format
- 680714162
- Labeler code
- 68071
- Product ID
- 68071-4162_bb632899-a752-7422-e053-2a95a90acc3a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ciclopirox olamine
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA076790
- Marketing category
- ANDA
- Marketing start
- 2005-04-12
- Marketing end
- 0000-00-00
- Substance
- CICLOPIROX OLAMINE
- Active strength
- 8 mg/g
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-4162-3 | 68071416203 | 30 g in 1 BOX (68071-4162-3) | 30 g | 2017-11-22 | 0000-00-00 | No | No | Current |