NDC 0378-4276 – Valacyclovir Hydrochloride
Valacyclovir Hydrochloride 1 g/1 · Tablet, Film Coated · Oral
Product NDC0378-4276
Product details
- Brand name
- Valacyclovir Hydrochloride
- Generic name
- valacyclovir
- Labeler
- Mylan Pharmaceuticals Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA078518
- 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
Uses, dosage, side effects and warnings for Valacyclovir Hydrochloride →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 0378-4276-77 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-4276-77) | May 24, 2010 |
| 0378-4276-93 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-4276-93) | May 24, 2010 |
Recalls mentioning this NDC
- D-0481-2024 May 8, 2024 · Class III
Failed Tablet/Capsule Specifications: There is a potential for the imprint, M 122, to be missing on some tablets.
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