Acyclovir
- Product NDC
- 70518-0798
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Acyclovir
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA074556
- Marketing category
- ANDA
- Substance
- ACYCLOVIR
- Current FDA listing
- Historical FDA.report record
Related Records
Packages
No records found.