FLUCYTOSINE
- Product NDC
- 42543-902
- 11-digit product format
- 425430902
- Labeler code
- 42543
- Product ID
- 42543-902_f44fbb3a-844b-4856-a2cc-257308cfa808
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- FLUCYTOSINE
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Vensun Pharmaceuticals, Inc.
- Application
- ANDA207536
- Marketing category
- ANDA
- Marketing start
- 2016-08-21
- Marketing end
- 0000-00-00
- Substance
- FLUCYTOSINE
- Active strength
- 250 mg/1
- Pharmacologic classes
- Nucleoside Analog [EXT],Nucleoside Analog Antifungal [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 42543-902-01 | 42543090201 | 100 CAPSULE in 1 BOTTLE (42543-902-01) | 100 capsule | 2016-08-21 | 0000-00-00 | No | No | Current |