Valacyclovir 63304-0904
Product NDC
63304-0904- Manufacturer
- Sun Pharmaceutical Industries, Inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- December 19, 2020
- Listing Expires
- December 31, 2026
- Application
- ANDA076588
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Valacyclovir Hydrochloride | 500 mg/1 |
Drug Class
DNA Polymerase Inhibitors [MoA]Herpes Simplex Virus Nucleoside Analog DNA Polymerase Inhibitor [EPC]Herpes Zoster Virus Nucleoside Analog DNA Polymerase Inhibitor [EPC]
Packaging Options(5)
10 TABLET, FILM COATED in 1 BOTTLE (63304-904-03)
500 TABLET, FILM COATED in 1 BOTTLE (63304-904-05)
30 TABLET, FILM COATED in 1 BOTTLE (63304-904-30)
100 BLISTER PACK in 1 CARTON (63304-904-77) / 1 TABLET, FILM COATED in 1 BLISTER PACK (63304-904-11)
90 TABLET, FILM COATED in 1 BOTTLE (63304-904-90)