acyclovir
- Product NDC
- 68071-3909
- 11-digit product format
- 680713909
- Labeler code
- 68071
- Product ID
- 68071-3909_41d5ae23-2733-325f-e063-6294a90ab07c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- acyclovir
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Labeler
- NuCare Pharmaceuticals, Inc.
- Application
- ANDA205510
- Marketing category
- ANDA
- Marketing start
- 2017-07-31
- 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 |
|---|
| 68071-3909-5 | 68071390905 | 1 TUBE in 1 CARTON (68071-3909-5) / 15 g in 1 TUBE | 1 tube | 2025-10-23 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Acyclovir Ointment USP, 5% | NuCare Pharmaceuticals, Inc. | 2025-10-23 | HUMAN PRESCRIPTION DRUG LABEL | 3 |