Prescription drug · ANDA
Acyclovir NDC 70518-4414
Acyclovir 400 mg/1 · Tablet · Oral · REMEDYREPACK INC.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 70518-4414-0 | 70518441400 | 30 TABLET in 1 BLISTER PACK (70518-4414-0)Marketed from Jul 31, 2025 |
How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules
Product information
- Brand name (proprietary)
- Acyclovir
- Generic name (nonproprietary)
- acyclovir
- Active ingredients
- Acyclovir — 400 mg/1
- Dosage form
- Tablet
- Route
- Oral
- Labeler
- REMEDYREPACK INC.
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 209366
- Marketing start
- Listing expires
- Other FDA classes
- DNA Polymerase Inhibitors (Mechanism)Nucleoside Analog (EXT)
- Identifiers
- Product ID 70518-4414_5b23a83c-14e9-f7eb-e063-6294a90a97a5SPL ID 5b23a83c-14e9-f7eb-e063-6294a90a97a5
- Pharmacologic class
- Herpes Simplex Virus Nucleoside Analog DNA Polymerase Inhibitor; Herpes Zoster Virus Nucleoside Analog DNA Polymerase Inhibitor; Herpesvirus Nucleoside Analog DNA Polymerase Inhibitor
Billing references
What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.
- HCPCS codeNo match
No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.
- NDC on a medical claim
N470518441400followed by a unit qualifier and the quantityPackage 70518-4414-00. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier
Product label
The FDA listing for this product does not reference a label (SPL) set.
Other NDCs under ANDA 209366
Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.
| Product | Strength | Form · route | Labeler | Product NDC |
|---|---|---|---|---|
| Acyclovir | Acyclovir 800 mg/1 | TabletOral | Bryant Ranch Prepack | 71335-2555 |
| Acyclovir | Acyclovir 800 mg/1 | TabletOral | SQUARE PHARMACEUTICALS LIMITED | 76483-042 |
| Acyclovir | Acyclovir 400 mg/1 | TabletOral | SQUARE PHARMACEUTICALS LIMITED | 76483-047 |
| Acyclovir | Acyclovir 400 mg/1 | TabletOral | Bionpharma Inc. | 69452-290 |
| Acyclovir | Acyclovir 800 mg/1 | TabletOral | Bionpharma Inc. | 69452-291 |
| Acyclovir | Acyclovir 400 mg/1 | TabletOral | NuCare Pharmaceuticals,Inc. | 68071-3573 |
| Acyclovir | Acyclovir 400 mg/1 | TabletOral | NuCare Pharmaceuticals,Inc. | 68071-2811 |
| Acyclovir | Acyclovir 800 mg/1 | TabletOral | REMEDYREPACK INC. | 70518-4450 |
| Acyclovir | Acyclovir 400 mg/1 | TabletOral | Bryant Ranch Prepack | 71335-2619 |
| Acyclovir | Acyclovir 400 mg/1 | TabletOral | Preferred Pharmaceuticals Inc. | 68788-8203 |
| Acyclovir | Acyclovir 800 mg/1 | TabletOral | A-S Medication Solutions | 50090-6335 |
| Acyclovir | Acyclovir 400 mg/1 | TabletOral | Direct_Rx | 72189-631 |
| Acyclovir | Acyclovir 400 mg/1 | TabletOral | Bryant Ranch Prepack | 71335-9620 |