acyclovir
- Product NDC
- 67296-1034
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- acyclovir
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- RedPharm Drug, 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 |
|---|
| 67296-1034-3 | 35 TABLET in 1 BOTTLE (67296-1034-3) | 2006-03-13 | 0000-00-00 | No | Current |
| 67296-1034-5 | 50 TABLET in 1 BOTTLE (67296-1034-5) | 2006-03-13 | 0000-00-00 | No | Current |
| 67296-1034-6 | 6 TABLET in 1 BOTTLE (67296-1034-6) | 2006-03-13 | 0000-00-00 | No | Current |