NDC 71335-2555 – Acyclovir
Acyclovir 800 mg/1 · Tablet · Oral
Product NDC71335-2555
Product details
- Brand name
- Acyclovir
- Generic name
- Acyclovir
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA209366
- Marketed since
- August 15, 2020
- Listing expires
- December 31, 2026
- Pharmacologic class
- Herpes Simplex Virus Nucleoside Analog DNA Polymerase Inhibitor; Herpes Zoster Virus Nucleoside Analog DNA Polymerase Inhibitor; Herpesvirus Nucleoside Analog DNA Polymerase Inhibitor
Active ingredients
- Acyclovir 800 mg/1
Package NDC codes (10)
| Package NDC | Description | Since |
|---|---|---|
| 71335-2555-0 | 500 TABLET in 1 BOTTLE (71335-2555-0) | Jan 23, 2025 |
| 71335-2555-1 | 25 TABLET in 1 BOTTLE (71335-2555-1) | Jan 23, 2025 |
| 71335-2555-2 | 35 TABLET in 1 BOTTLE (71335-2555-2) | Jan 23, 2025 |
| 71335-2555-3 | 30 TABLET in 1 BOTTLE (71335-2555-3) | Jan 23, 2025 |
| 71335-2555-4 | 60 TABLET in 1 BOTTLE (71335-2555-4) | Jan 23, 2025 |
| 71335-2555-5 | 50 TABLET in 1 BOTTLE (71335-2555-5) | Jan 23, 2025 |
| 71335-2555-6 | 10 TABLET in 1 BOTTLE (71335-2555-6) | Jan 23, 2025 |
| 71335-2555-7 | 40 TABLET in 1 BOTTLE (71335-2555-7) | Jan 23, 2025 |
| 71335-2555-8 | 21 TABLET in 1 BOTTLE (71335-2555-8) | Jan 23, 2025 |
| 71335-2555-9 | 90 TABLET in 1 BOTTLE (71335-2555-9) | Jan 23, 2025 |
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