NDC 65862-448 – Valacyclovir Hydrochloride
Valacyclovir Hydrochloride 500 mg/1 · Tablet, Film Coated · Oral
Product NDC65862-448
Product details
- Brand name
- Valacyclovir Hydrochloride
- Generic name
- Valacyclovir Hydrochloride
- Labeler
- Aurobindo Pharma Limited
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA090682
- Marketed since
- May 24, 2010
- Listing expires
- December 31, 2026
- 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 (6)
| Package NDC | Description | Since |
|---|---|---|
| 65862-448-01 | 100 TABLET, FILM COATED in 1 BOTTLE (65862-448-01) | May 24, 2010 |
| 65862-448-05 | 500 TABLET, FILM COATED in 1 BOTTLE (65862-448-05) | May 24, 2010 |
| 65862-448-10 | 10 BLISTER PACK in 1 CARTON (65862-448-10) / 10 TABLET, FILM COATED in 1 BLISTER PACK | May 24, 2010 |
| 65862-448-30 | 30 TABLET, FILM COATED in 1 BOTTLE (65862-448-30) | May 24, 2010 |
| 65862-448-35 | 3500 TABLET, FILM COATED in 1 BOTTLE (65862-448-35) | May 24, 2010 |
| 65862-448-90 | 90 TABLET, FILM COATED in 1 BOTTLE (65862-448-90) | May 24, 2010 |
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