NDC 71205-388 – Acyclovir
Acyclovir 800 mg/1 · Tablet · Oral
Product NDC71205-388
Product details
- Brand name
- Acyclovir
- Generic name
- Acyclovir
- Labeler
- Proficient Rx LP
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA074891
- Marketed since
- August 8, 2013
- 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 (4)
| Package NDC | Description | Since |
|---|---|---|
| 71205-388-30 | 30 TABLET in 1 BOTTLE (71205-388-30) | Feb 8, 2022 |
| 71205-388-35 | 35 TABLET in 1 BOTTLE (71205-388-35) | Feb 8, 2022 |
| 71205-388-60 | 60 TABLET in 1 BOTTLE (71205-388-60) | Feb 8, 2022 |
| 71205-388-90 | 90 TABLET in 1 BOTTLE (71205-388-90) | Feb 8, 2022 |
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