acyclovir
- Product NDC
- 70934-694
- 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 |
|---|
| 70934-694-25 | 25 TABLET in 1 BOTTLE, PLASTIC (70934-694-25) | 2020-05-04 | 0000-00-00 | No | Current |
| 70934-694-30 | 30 TABLET in 1 BOTTLE, PLASTIC (70934-694-30) | 2020-05-06 | 0000-00-00 | No | Current |
| 70934-694-45 | 45 TABLET in 1 BOTTLE, PLASTIC (70934-694-45) | 2020-05-04 | 0000-00-00 | No | Current |
| 70934-694-60 | 60 TABLET in 1 BOTTLE, PLASTIC (70934-694-60) | 2020-05-08 | 0000-00-00 | No | Current |
| 70934-694-90 | 90 TABLET in 1 BOTTLE, PLASTIC (70934-694-90) | 2020-05-14 | 0000-00-00 | No | Current |