Flucytosine
- Product NDC
- 60687-352
- 11-digit product format
- 606870352
- Labeler code
- 60687
- Product ID
- 60687-352_d61b7442-a7f8-62c4-e053-2a95a90ad9b4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Flucytosine
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- American Health Packaging
- Application
- ANDA204652
- Marketing category
- ANDA
- Marketing start
- 2018-01-15
- Marketing end
- 2022-08-31
- Substance
- FLUCYTOSINE
- Active strength
- 250 mg/1
- Pharmacologic classes
- Nucleoside Analog Antifungal [EPC], Nucleoside Analog [EXT]
- 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 |
|---|
| 60687-352-25 | 60687035225 | 30 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-352-25) > 1 CAPSULE in 1 BLISTER PACK (60687-352-95) | 30 blister pack | 2018-01-15 | 0000-00-00 | No | No | Current |