NDC 71205-609 – Famciclovir
Famciclovir 500 mg/1 · Tablet, Film Coated · Oral
Product NDC71205-609
Product details
- Brand name
- Famciclovir
- Generic name
- Famciclovir
- Labeler
- Proficient Rx LP
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA201022
- Marketed since
- January 13, 2012
- Listing expires
- December 31, 2026
- Pharmacologic class
- Herpesvirus Nucleoside Analog DNA Polymerase Inhibitor
Active ingredients
- Famciclovir 500 mg/1
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 71205-609-21 | 21 TABLET, FILM COATED in 1 BOTTLE (71205-609-21) | Oct 4, 2021 |
| 71205-609-30 | 30 TABLET, FILM COATED in 1 BOTTLE (71205-609-30) | Oct 4, 2021 |
| 71205-609-60 | 60 TABLET, FILM COATED in 1 BOTTLE (71205-609-60) | Oct 4, 2021 |
| 71205-609-90 | 90 TABLET, FILM COATED in 1 BOTTLE (71205-609-90) | Oct 4, 2021 |
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