FAMCICLOVIR
- Product NDC
- 69097-271
- 11-digit product format
- 690970271
- Labeler code
- 69097
- Product ID
- 69097-271_5a272fa6-6d28-4a21-b6b4-f01079684ee2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Famciclovir
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Cipla USA Inc.
- Application
- ANDA078278
- Marketing category
- ANDA
- Marketing start
- 2011-03-21
- Marketing end
- 2022-03-31
- 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
- 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 |
|---|
| 69097-271-02 | 69097027102 | 30 TABLET in 1 BOTTLE (69097-271-02) | 30 tablet | 2011-03-21 | 2022-03-31 | No | No | Current |