acyclovir
- Product NDC
- 68788-7895
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- acyclovir
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA077309
- Marketing category
- ANDA
- Substance
- ACYCLOVIR
- Current FDA listing
- Historical FDA.report record
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 68788-7895-2 | 21 TABLET in 1 BOTTLE (68788-7895-2) | 2021-04-29 | 0000-00-00 | No | Current |
| 68788-7895-3 | 30 TABLET in 1 BOTTLE (68788-7895-3) | 2021-04-29 | 0000-00-00 | No | Current |
| 68788-7895-4 | 40 TABLET in 1 BOTTLE (68788-7895-4) | 2021-04-29 | 0000-00-00 | No | Current |
| 68788-7895-5 | 50 TABLET in 1 BOTTLE (68788-7895-5) | 2021-04-29 | 0000-00-00 | No | Current |