Valacyclovir Hydrochloride
- Product NDC
- 50090-2224
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Valacyclovir Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA090682
- Marketing category
- ANDA
- Substance
- VALACYCLOVIR HYDROCHLORIDE
- Current FDA listing
- Historical FDA.report record
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 50090-2224-0 | 10 TABLET, FILM COATED in 1 BOTTLE (50090-2224-0) | 2015-11-09 | 0000-00-00 | No | Current |
| 50090-2224-1 | 14 TABLET, FILM COATED in 1 BOTTLE (50090-2224-1) | 2015-11-09 | 0000-00-00 | No | Current |
| 50090-2224-2 | 30 TABLET, FILM COATED in 1 BOTTLE (50090-2224-2) | 2015-11-09 | 0000-00-00 | No | Current |
| 50090-2224-3 | 90 TABLET, FILM COATED in 1 BOTTLE (50090-2224-3) | 2017-01-04 | 0000-00-00 | No | Current |