acyclovir
- Product NDC
- 68071-5094
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- acyclovir
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- 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 |
|---|---|---|---|---|---|
| 68071-5094-1 | 100 TABLET in 1 BOTTLE (68071-5094-1) | 2019-10-25 | 0000-00-00 | No | Current |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|---|---|---|---|
| ACYCLOVIR TABLETS, USP 400 mg and 800 mg | NuCare Pharmaceuticals,Inc. | 2021-02-22 | HUMAN PRESCRIPTION DRUG LABEL | 2 |