acyclovir
- Product NDC
- 70934-697
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- acyclovir
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Apotex Corp.
- Application
- ANDA077309
- Marketing category
- ANDA
- Substance
- ACYCLOVIR
- Current FDA listing
- Historical FDA.report record
Related Records
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|---|---|---|---|---|
| 70934-697-35 | 35 TABLET in 1 BOTTLE, PLASTIC (70934-697-35) | 2020-05-08 | 0000-00-00 | No | Current |
| 70934-697-70 | 70 TABLET in 1 BOTTLE, PLASTIC (70934-697-70) | 2020-05-12 | 0000-00-00 | No | Current |