Fluconazole
- Product NDC
- 55154-7138
- 11-digit product format
- 551547138
- Labeler code
- 55154
- Product ID
- 55154-7138_99911052-a041-4d1f-b18f-1bf4b9ef6731
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Fluconazole
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Cardinal Health
- Application
- ANDA077731
- Marketing category
- ANDA
- Marketing start
- 2015-08-11
- Marketing end
- 2021-03-31
- Substance
- FLUCONAZOLE
- Active strength
- 200 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
- 0000-00-00
- 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 |
|---|
| 55154-7138-0 | 55154713800 | 10 BLISTER PACK in 1 BAG (55154-7138-0) > 1 TABLET in 1 BLISTER PACK | 10 blister pack | 2015-08-11 | 2021-03-31 | No | No | Current |