acyclovir
- Product NDC
- 70518-0427
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- acyclovir
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA077309
- Marketing category
- ANDA
- Substance
- ACYCLOVIR
- Current FDA listing
- Yes
Related Records
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|---|---|---|---|---|
| 70518-0427-1 | 30 TABLET in 1 BOTTLE, PLASTIC (70518-0427-1) | 2017-04-21 | 2026-12-31 | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|---|---|---|---|
| ACYCLOVIR TABLETS, USP 400 mg and 800 mg | REMEDYREPACK INC. | 2026-01-05 | HUMAN PRESCRIPTION DRUG LABEL | 18 |