acyclovir
- Product NDC
- 50090-0643
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- acyclovir
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- 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 |
|---|---|---|---|---|---|
| 50090-0643-0 | 90 TABLET in 1 BOTTLE (50090-0643-0) | 2014-11-28 | 0000-00-00 | No | Current |
| 50090-0643-1 | 21 TABLET in 1 BOTTLE (50090-0643-1) | 2019-10-23 | 0000-00-00 | No | Current |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|---|---|---|---|
| ACYCLOVIR TABLETS, USP 400 mg and 800 mg | A-S Medication Solutions | 2021-03-17 | HUMAN PRESCRIPTION DRUG LABEL | 2 |