Valacyclovir Hydrochloride
- Product NDC
- 60760-757
- 11-digit product format
- 607600757
- Labeler code
- 60760
- Product ID
- 60760-757_275c0198-10a6-139e-e063-6394a90a72be
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Valacyclovir Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- ST. MARY'S MEDICAL PARK PHARMACY
- Application
- ANDA090682
- Marketing category
- ANDA
- Marketing start
- 2010-05-24
- Substance
- VALACYCLOVIR HYDROCHLORIDE
- Active strength
- 1 g/1
- Pharmacologic classes
- DNA Polymerase Inhibitors [MoA], Herpes Simplex Virus Nucleoside Analog DNA Polymerase Inhibitor [EPC], Herpes Zoster Virus Nucleoside Analog DNA Polymerase Inhibitor [EPC], Herpesvirus Nucleoside Analog DNA Polymerase Inhibitor [EPC], Nucleoside Analog [EXT]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| G447S0T1VC | VALACYCLOVIR HYDROCHLORIDE | 124832-27-5 | VALACYCLOVIR HYDROCHLORIDE |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 60760-757-42 | 60760075742 | 42 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-757-42) | 2024-11-14 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Valacyclovir Hydrochloride | ST. MARY'S MEDICAL PARK PHARMACY | 2024-11-20 | HUMAN PRESCRIPTION DRUG LABEL | 1 |