acyclovir
- Product NDC
- 63187-192
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- acyclovir
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA077309
- Marketing category
- ANDA
- Substance
- ACYCLOVIR
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 63187-192-30 | 30 TABLET in 1 BOTTLE (63187-192-30) | 2019-01-01 | | No | Historical |
| 63187-192-35 | 35 TABLET in 1 BOTTLE (63187-192-35) | 2019-01-01 | | No | Historical |
| 63187-192-60 | 60 TABLET in 1 BOTTLE (63187-192-60) | 2019-01-01 | | No | Historical |
| 63187-192-90 | 90 TABLET in 1 BOTTLE (63187-192-90) | 2019-01-01 | | No | Historical |