voriconazole
- Product NDC
- 51407-133
- 11-digit product format
- 514070133
- Labeler code
- 51407
- Product ID
- 51407-133_efbbeda7-6bf9-13ca-e053-2995a90a4177
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- voriconazole
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Golden State Medical Supply, Inc.
- Application
- ANDA203503
- Marketing category
- ANDA
- Marketing start
- 2015-09-02
- Marketing end
- 0000-00-00
- Substance
- VORICONAZOLE
- Active strength
- 200 mg/1
- Pharmacologic classes
- Azole Antifungal [EPC], Azoles [CS], Cytochrome P450 2C19 Inhibitors [MoA], Cytochrome P450 2C9 Inhibitors [MoA], Cytochrome P450 3A4 Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 51407-133-30 | 51407013330 | 30 TABLET, FILM COATED in 1 BOTTLE (51407-133-30) | 2018-09-05 | 0000-00-00 | No | No | Current |