acyclovir
- Product NDC
- 63629-7975
- 11-digit product format
- 636297975
- Labeler code
- 63629
- Product ID
- 63629-7975_6c990a79-2585-41ce-b48e-c2e748976f9a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- acyclovir
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA204314
- Marketing category
- ANDA
- Marketing start
- 2014-09-10
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 63629-7975-1 | 63629797501 | 40 TABLET in 1 BOTTLE (63629-7975-1) | 40 tablet | 2019-03-28 | 0000-00-00 | No | No | Current |
| 63629-7975-2 | 63629797502 | 35 TABLET in 1 BOTTLE (63629-7975-2) | 35 tablet | 2019-03-28 | 0000-00-00 | No | No | Current |