NDC 71335-1222 – Acyclovir
Acyclovir 800 mg/1 · Tablet · Oral
Product NDC71335-1222
Product details
- Brand name
- Acyclovir
- Generic name
- Acyclovir
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA210401
- Marketed since
- May 4, 2018
- 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 |
|---|---|---|
| 71335-1222-0 | 500 TABLET in 1 BOTTLE (71335-1222-0) | Jan 30, 2025 |
| 71335-1222-1 | 25 TABLET in 1 BOTTLE (71335-1222-1) | Jun 7, 2019 |
| 71335-1222-2 | 35 TABLET in 1 BOTTLE (71335-1222-2) | Jun 3, 2019 |
| 71335-1222-3 | 30 TABLET in 1 BOTTLE (71335-1222-3) | May 13, 2019 |
| 71335-1222-4 | 60 TABLET in 1 BOTTLE (71335-1222-4) | Jan 30, 2025 |
| 71335-1222-5 | 50 TABLET in 1 BOTTLE (71335-1222-5) | May 6, 2019 |
| 71335-1222-6 | 10 TABLET in 1 BOTTLE (71335-1222-6) | Jan 30, 2025 |
| 71335-1222-7 | 40 TABLET in 1 BOTTLE (71335-1222-7) | May 23, 2019 |
| 71335-1222-8 | 21 TABLET in 1 BOTTLE (71335-1222-8) | Jan 30, 2025 |
| 71335-1222-9 | 90 TABLET in 1 BOTTLE (71335-1222-9) | Jan 30, 2025 |
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