Valacyclovir Hydrochloride
- Product NDC
- 72789-263
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Valacyclovir Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- ANDA090682
- Marketing category
- ANDA
- Substance
- VALACYCLOVIR HYDROCHLORIDE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 72789-263-06 | 6 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-263-06) | 2025-06-18 | | No | Historical |
| 72789-263-10 | 10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-263-10) | 2022-10-11 | | No | Historical |
| 72789-263-14 | 14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-263-14) | 2023-12-04 | | No | Historical |
| 72789-263-28 | 28 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-263-28) | 2025-03-03 | | No | Historical |
| 72789-263-90 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-263-90) | 2022-07-20 | | No | Historical |