FAMCICLOVIR
- Product NDC
- 63187-920
- 11-digit product format
- 631870920
- Labeler code
- 63187
- Product ID
- 63187-920_fe188ea7-a1f6-4139-9679-3c07130cfc4f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Famciclovir
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA078278
- Marketing category
- ANDA
- Marketing start
- 2011-03-21
- Marketing end
- 0000-00-00
- Substance
- FAMCICLOVIR
- Active strength
- 500 mg/1
- Pharmacologic classes
- DNA Polymerase Inhibitors [MoA],Herpesvirus Nucleoside Analog DNA Polymerase Inhibitor [EPC],Nucleoside Analog [EXT]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 63187-920 | FAMCICLOVIR TABLET [PROFICIENT RX LP] | 3 | Legacy NDC | 20191108_dc35c263-831b-4d57-9834-07363972648e.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63187-920-21 | 63187092021 | 21 TABLET in 1 BOTTLE (63187-920-21) | 21 tablet | 2017-10-02 | 0000-00-00 | No | No | Current |
| 63187-920-30 | 63187092030 | 30 TABLET in 1 BOTTLE (63187-920-30) | 30 tablet | 2017-10-02 | 0000-00-00 | No | No | Current |
| 63187-920-60 | 63187092060 | 60 TABLET in 1 BOTTLE (63187-920-60) | 60 tablet | 2017-10-02 | 0000-00-00 | No | No | Current |
| 63187-920-90 | 63187092090 | 90 TABLET in 1 BOTTLE (63187-920-90) | 90 tablet | 2017-10-02 | 0000-00-00 | No | No | Current |