Acyclovir
- Product NDC
- 71335-2229
- 11-digit product format
- 713352229
- Labeler code
- 71335
- Product ID
- 71335-2229_b182ebdb-eadd-4688-a71f-587fba8f1964
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Acyclovir
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA075382
- Marketing category
- ANDA
- Marketing start
- 2009-10-22
- 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
- 2026-12-31
- Current FDA listing
- Yes
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 | Sample | Exclude flag | Status |
|---|
| 71335-2229-1 | 71335222901 | 35 TABLET in 1 BOTTLE, PLASTIC (71335-2229-1) | 35 tablet | 2024-09-06 | No | No | Historical |
| 71335-2229-2 | 71335222902 | 90 TABLET in 1 BOTTLE, PLASTIC (71335-2229-2) | 90 tablet | 2023-08-23 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Acyclovir Tablets USP | Bryant Ranch Prepack | 2024-09-06 | HUMAN PRESCRIPTION DRUG LABEL | 101 |