acyclovir
- Product NDC
- 68788-7760
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- acyclovir
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals, 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 |
|---|
| 68788-7760-1 | 100 TABLET in 1 BOTTLE (68788-7760-1) | 2020-07-01 | 0000-00-00 | No | Current |
| 68788-7760-2 | 21 TABLET in 1 BOTTLE (68788-7760-2) | 2020-07-01 | 0000-00-00 | No | Current |
| 68788-7760-3 | 30 TABLET in 1 BOTTLE (68788-7760-3) | 2020-07-01 | 0000-00-00 | No | Current |
| 68788-7760-4 | 40 TABLET in 1 BOTTLE (68788-7760-4) | 2020-07-01 | 0000-00-00 | No | Current |
| 68788-7760-5 | 50 TABLET in 1 BOTTLE (68788-7760-5) | 2020-07-01 | 0000-00-00 | No | Current |
| 68788-7760-6 | 60 TABLET in 1 BOTTLE (68788-7760-6) | 2020-07-01 | 0000-00-00 | No | Current |
| 68788-7760-7 | 28 TABLET in 1 BOTTLE (68788-7760-7) | 2020-07-01 | 0000-00-00 | No | Current |
| 68788-7760-8 | 35 TABLET in 1 BOTTLE (68788-7760-8) | 2020-07-01 | 0000-00-00 | No | Current |
| 68788-7760-9 | 45 TABLET in 1 BOTTLE (68788-7760-9) | 2020-07-01 | 0000-00-00 | No | Current |