NDC 31722-706 – Famciclovir
Famciclovir 125 mg/1 · Tablet, Film Coated · Oral
Product NDC31722-706
Product details
- Brand name
- Famciclovir
- Generic name
- Famciclovir
- Labeler
- Camber Pharmaceuticals, Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA202438
- Marketed since
- September 10, 2014
- Listing expires
- December 31, 2026
- Pharmacologic class
- Herpesvirus Nucleoside Analog DNA Polymerase Inhibitor
Active ingredients
- Famciclovir 125 mg/1
Package NDC codes (5)
| Package NDC | Description | Since |
|---|---|---|
| 31722-706-01 | 100 TABLET, FILM COATED in 1 BOTTLE (31722-706-01) | Sep 10, 2014 |
| 31722-706-05 | 500 TABLET, FILM COATED in 1 BOTTLE (31722-706-05) | Sep 10, 2014 |
| 31722-706-10 | 1000 TABLET, FILM COATED in 1 BOTTLE (31722-706-10) | Sep 10, 2014 |
| 31722-706-30 | 30 TABLET, FILM COATED in 1 BOTTLE (31722-706-30) | Sep 10, 2014 |
| 31722-706-60 | 60 TABLET, FILM COATED in 1 BOTTLE (31722-706-60) | Sep 10, 2014 |
Recalls mentioning this NDC
- D-0415-2018 Feb 21, 2018 · Class II
Temperature Abuse: Complaints of tablets being wet and stuck together with tablet coating peeled and disintegrated as a result of prolonged exposure to high temp during distribution.
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