Flucytosine
- Product NDC
- 63629-9291
- 11-digit product format
- 636299291
- Labeler code
- 63629
- Product ID
- 63629-9291_a3d92129-24cd-41ee-9815-404e3ece4aec
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Flucytosine
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- NDA017001
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2017-07-26
- Marketing end
- 0000-00-00
- Substance
- FLUCYTOSINE
- Active strength
- 250 mg/1
- Pharmacologic classes
- Nucleoside Analog Antifungal [EPC], Nucleoside Analog [EXT]
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-9291-1 | 63629929101 | 100 CAPSULE in 1 BOTTLE (63629-9291-1) | 100 capsule | 2022-06-06 | 0000-00-00 | No | No | Current |