Acyclovir
- Product NDC
- 70771-1808
- 11-digit product format
- 707711808
- Labeler code
- 70771
- Product ID
- 70771-1808_400d6da5-8a57-4156-a3ef-4aaacfe2d7ef
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Acyclovir
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Zydus Lifesciences Limited
- Application
- ANDA206770
- Marketing category
- ANDA
- Marketing start
- 2023-03-03
- 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 |
|---|
| 70771-1808-2 | 70771180802 | 1 TUBE in 1 CARTON (70771-1808-2) / 2 g in 1 TUBE | 1 tube | 2023-03-03 | No | No | Historical |
| 70771-1808-5 | 70771180805 | 1 TUBE in 1 CARTON (70771-1808-5) / 5 g in 1 TUBE | 1 tube | 2023-03-03 | No | No | Historical |