acyclovir
- Product NDC
- 70934-556
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- acyclovir
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Denton Pharma, Inc. DBA Northwind Pharmaceuticals
- Application
- ANDA077309
- Marketing category
- ANDA
- Substance
- ACYCLOVIR
- Current FDA listing
- Historical FDA.report record
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 70934-556-35 | 35 TABLET in 1 BOTTLE, PLASTIC (70934-556-35) | 2020-02-19 | 0000-00-00 | No | Current |
| 70934-556-40 | 40 TABLET in 1 BOTTLE, PLASTIC (70934-556-40) | 2020-03-12 | 0000-00-00 | No | Current |