NDC 72162-1724 – Acyclovir
Acyclovir 800 mg/1 · Tablet · Oral
Product NDC72162-1724
Product details
- Brand name
- Acyclovir
- Generic name
- Acyclovir
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA077309
- Marketed since
- March 13, 2006
- Marketing end
- 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 |
|---|---|---|
| 72162-1724-0 | 40 TABLET in 1 BOTTLE (72162-1724-0) | Aug 12, 2024 |
| 72162-1724-1 | 21 TABLET in 1 BOTTLE (72162-1724-1) | Aug 12, 2024 |
| 72162-1724-2 | 25 TABLET in 1 BOTTLE (72162-1724-2) | Aug 12, 2024 |
| 72162-1724-3 | 30 TABLET in 1 BOTTLE (72162-1724-3) | Aug 12, 2024 |
| 72162-1724-4 | 35 TABLET in 1 BOTTLE (72162-1724-4) | Aug 12, 2024 |
| 72162-1724-5 | 500 TABLET in 1 BOTTLE (72162-1724-5) | Aug 12, 2024 |
| 72162-1724-6 | 60 TABLET in 1 BOTTLE (72162-1724-6) | Aug 12, 2024 |
| 72162-1724-7 | 50 TABLET in 1 BOTTLE (72162-1724-7) | Aug 12, 2024 |
| 72162-1724-8 | 10 TABLET in 1 BOTTLE (72162-1724-8) | Aug 12, 2024 |
| 72162-1724-9 | 90 TABLET in 1 BOTTLE (72162-1724-9) | Aug 12, 2024 |
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