Acyclovir
- Product NDC
- 63629-6349
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Acyclovir
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA074556
- Marketing category
- ANDA
- Substance
- ACYCLOVIR
- Current FDA listing
- Historical FDA.report record
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 63629-6349-1 | 30 TABLET in 1 BOTTLE (63629-6349-1) | 2015-09-04 | 0000-00-00 | No | Current |
| 63629-6349-2 | 35 TABLET in 1 BOTTLE (63629-6349-2) | 2015-09-28 | 0000-00-00 | No | Current |
| 63629-6349-3 | 50 TABLET in 1 BOTTLE (63629-6349-3) | 2016-05-16 | 0000-00-00 | No | Current |