ACYCLOVIR
- Product NDC
- 70934-532
- 11-digit product format
- 709340532
- Labeler code
- 70934
- Product ID
- 70934-532_a9cbbf46-74fe-6dea-e053-2995a90a683f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ACYCLOVIR
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Denton Pharma, Inc. DBA Northwind Pharmaceuticals
- Application
- ANDA074891
- Marketing category
- ANDA
- Marketing start
- 2020-02-17
- Marketing end
- 0000-00-00
- Substance
- ACYCLOVIR
- Active strength
- 800 mg/1
- Pharmacologic classes
- DNA Polymerase Inhibitors [MoA],Herpes Simplex Virus Nucleoside Analog DNA Polymerase Inhibitor [EPC],Herpes Zoster Virus Nucleoside Analog DNA Polymerase Inhibitor [EPC],Herpesvirus Nucleoside Analog DNA Polymerase Inhibitor [EPC],Nucleoside Analog [EXT]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| X4HES1O11F | ACYCLOVIR | 59277-89-3 | ACYCLOVIR |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70934-532-70 | 70934053270 | 70 TABLET in 1 BOTTLE, PLASTIC (70934-532-70) | 70 tablet | 2020-02-17 | 0000-00-00 | No | No | Current |