Acyclovir
- Product NDC
- 72162-1960
- 11-digit product format
- 721621960
- Labeler code
- 72162
- Product ID
- 72162-1960_6728b8ab-62f7-468e-8515-b5b13013c2ad
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Acyclovir
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA201501
- Marketing category
- ANDA
- Marketing start
- 2020-01-30
- Substance
- ACYCLOVIR
- Active strength
- 50 mg/g
- 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 |
|---|
| 72162-1960-2 | 72162196002 | 15 g in 1 TUBE (72162-1960-2) | 15 g | 2024-01-25 | No | No | Historical |
| 72162-1960-3 | 72162196003 | 30 g in 1 TUBE (72162-1960-3) | 30 g | 2024-01-25 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Acyclovir Ointment USP, 5% | Bryant Ranch Prepack | 2024-01-25 | HUMAN PRESCRIPTION DRUG LABEL | 100 |