Fluconazole
- Product NDC
- 68071-2114
- 11-digit product format
- 680712114
- Labeler code
- 68071
- Product ID
- 68071-2114_a731cba0-749c-98ac-e053-2a95a90a28ec
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Fluconazole
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA077253
- Marketing category
- ANDA
- Marketing start
- 2006-01-25
- Marketing end
- 0000-00-00
- Substance
- FLUCONAZOLE
- Active strength
- 150 mg/1
- Pharmacologic classes
- Azole Antifungal [EPC],Azoles [CS],Cytochrome P450 2C19 Inhibitors [MoA],Cytochrome P450 3A4 Inhibitors [MoA],Cytochrome P450 2C9 Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 68071-2114-2 | 68071211402 | 2 TABLET in 1 BLISTER PACK (68071-2114-2) | 2 tablet | 2020-06-03 | 0000-00-00 | No | No | Current |