NDC 70518-2266 – Valacyclovir Hydrochloride
Valacyclovir Hydrochloride 500 mg/1 · Tablet, Film Coated · Oral
Product NDC70518-2266
Product details
- Brand name
- Valacyclovir Hydrochloride
- Generic name
- Valacyclovir Hydrochloride
- Labeler
- REMEDYREPACK INC.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA090682
- Marketed since
- August 15, 2019
- 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
Uses, dosage, side effects and warnings for Valacyclovir Hydrochloride →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 70518-2266-0 | 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2266-0) | Aug 15, 2019 |
| 70518-2266-1 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2266-1) | May 26, 2021 |
| 70518-2266-2 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2266-2) | Jul 6, 2021 |
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