Valacyclovir Hydrochloride
- Product NDC
- 82804-093
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Valacyclovir Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA090682
- Marketing category
- ANDA
- Substance
- VALACYCLOVIR HYDROCHLORIDE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 82804-093-10 | 10 TABLET, FILM COATED in 1 BOTTLE (82804-093-10) | 2024-07-19 | | No | Historical |
| 82804-093-14 | 14 TABLET, FILM COATED in 1 BOTTLE (82804-093-14) | 2026-01-13 | | No | Historical |
| 82804-093-21 | 21 TABLET, FILM COATED in 1 BOTTLE (82804-093-21) | 2024-04-05 | | No | Historical |
| 82804-093-30 | 30 TABLET, FILM COATED in 1 BOTTLE (82804-093-30) | 2024-04-02 | | No | Historical |