ACYCLOVIR
- Product NDC
- 70934-465
- 11-digit product format
- 709340465
- Labeler code
- 70934
- Product ID
- 70934-465_a14042bf-5316-11c0-e053-2a95a90aca1b
- 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
- 2019-11-26
- Marketing end
- 0000-00-00
- Substance
- ACYCLOVIR
- Active strength
- 400 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
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 70934-465-30 | 70934046530 | 30 TABLET in 1 BOTTLE, PLASTIC (70934-465-30) | 30 tablet | 2019-11-26 | 0000-00-00 | No | No | Current |
| 70934-465-60 | 70934046560 | 60 TABLET in 1 BOTTLE, PLASTIC (70934-465-60) | 60 tablet | 2020-01-08 | 0000-00-00 | No | No | Current |