Famciclovir
- Product NDC
- 16714-615
- 11-digit product format
- 167140615
- Labeler code
- 16714
- Product ID
- 16714-615_f0d6104e-244c-40fb-b06c-d395e0f9f1a8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Famciclovir
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NorthStar RxLLC
- Application
- ANDA078278
- Marketing category
- ANDA
- Marketing start
- 2017-02-01
- Marketing end
- 0000-00-00
- Substance
- FAMCICLOVIR
- Active strength
- 250 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
- 2021-12-31
- 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 |
|---|
| 16714-615-01 | 16714061501 | 30 TABLET in 1 BOTTLE (16714-615-01) | 30 tablet | 2017-02-01 | 0000-00-00 | No | No | Current |