NDC 72789-263 – Valacyclovir Hydrochloride
Valacyclovir Hydrochloride 500 mg/1 · Tablet, Film Coated · Oral
Product NDC72789-263
Product details
- Brand name
- Valacyclovir Hydrochloride
- Generic name
- Valacyclovir Hydrochloride
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA090682
- Marketed since
- May 24, 2010
- 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 (5)
| Package NDC | Description | Since |
|---|---|---|
| 72789-263-06 | 6 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-263-06) | Jun 18, 2025 |
| 72789-263-10 | 10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-263-10) | Oct 11, 2022 |
| 72789-263-14 | 14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-263-14) | Dec 4, 2023 |
| 72789-263-28 | 28 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-263-28) | Mar 3, 2025 |
| 72789-263-90 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-263-90) | Jul 20, 2022 |
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