NDC 68084-215 – Valacyclovir Hydrochloride
Valacyclovir Hydrochloride 500 mg/1 · Tablet, Film Coated · Oral
Product NDC68084-215
Product details
- Brand name
- Valacyclovir Hydrochloride
- Generic name
- Valacyclovir Hydrochloride
- Labeler
- American Health Packaging
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA090682
- Marketed since
- August 20, 2014
- 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 (2)
| Package NDC | Description | Since |
|---|---|---|
| 68084-215-01 | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-215-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-215-11) | Aug 20, 2014 |
| 68084-215-21 | 30 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-215-21) / 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-215-11) | Jul 28, 2021 |
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