NDC 71335-1053 – Acyclovir
Acyclovir 400 mg/1 · Tablet · Oral
Product NDC71335-1053
Product details
- Brand name
- Acyclovir
- Generic name
- Acyclovir
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA075382
- Marketed since
- October 22, 2009
- 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 400 mg/1
Package NDC codes (10)
| Package NDC | Description | Since |
|---|---|---|
| 71335-1053-0 | 120 TABLET in 1 BOTTLE (71335-1053-0) | Nov 13, 2019 |
| 71335-1053-1 | 20 TABLET in 1 BOTTLE (71335-1053-1) | Feb 19, 2019 |
| 71335-1053-2 | 28 TABLET in 1 BOTTLE (71335-1053-2) | Feb 6, 2020 |
| 71335-1053-3 | 30 TABLET in 1 BOTTLE (71335-1053-3) | Jan 28, 2019 |
| 71335-1053-4 | 50 TABLET in 1 BOTTLE (71335-1053-4) | Jan 15, 2019 |
| 71335-1053-5 | 15 TABLET in 1 BOTTLE (71335-1053-5) | Jun 1, 2020 |
| 71335-1053-6 | 60 TABLET in 1 BOTTLE (71335-1053-6) | Jan 8, 2019 |
| 71335-1053-7 | 25 TABLET in 1 BOTTLE (71335-1053-7) | Mar 2, 2021 |
| 71335-1053-8 | 10 TABLET in 1 BOTTLE (71335-1053-8) | Jan 3, 2020 |
| 71335-1053-9 | 40 TABLET in 1 BOTTLE (71335-1053-9) | Aug 24, 2022 |
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