NDC 63304-904 – Valacyclovir
Valacyclovir Hydrochloride 500 mg/1 · Tablet, Film Coated · Oral
Product NDC63304-904
Product details
- Brand name
- Valacyclovir
- Generic name
- Valacyclovir
- Labeler
- SUN PHARMACEUTICAL INDUSTRIES, INC.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA076588
- Marketed since
- December 19, 2020
- Listing expires
- December 31, 2027
- Pharmacologic class
- Herpes Simplex Virus Nucleoside Analog DNA Polymerase Inhibitor; Herpes Zoster Virus Nucleoside Analog DNA Polymerase Inhibitor; Herpesvirus Nucleoside Analog DNA Polymerase Inhibitor
Active ingredients
- Valacyclovir Hydrochloride 500 mg/1
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 63304-904-03 | 10 TABLET, FILM COATED in 1 BOTTLE (63304-904-03) | Dec 19, 2020 |
| 63304-904-05 | 500 TABLET, FILM COATED in 1 BOTTLE (63304-904-05) | Dec 19, 2020 |
| 63304-904-77 | 100 BLISTER PACK in 1 CARTON (63304-904-77) / 1 TABLET, FILM COATED in 1 BLISTER PACK (63304-904-11) | Dec 19, 2020 |
| 63304-904-90 | 90 TABLET, FILM COATED in 1 BOTTLE (63304-904-90) | Dec 19, 2020 |
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