NDC 71205-391 – acyclovir
Acyclovir 400 mg/1 · Tablet · Oral
Product NDC71205-391
Product details
- Brand name
- acyclovir
- Generic name
- acyclovir
- Labeler
- Proficient Rx LP
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA077309
- Marketed since
- June 9, 2007
- 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 (4)
| Package NDC | Description | Since |
|---|---|---|
| 71205-391-25 | 25 TABLET in 1 BOTTLE (71205-391-25) | Jan 28, 2020 |
| 71205-391-30 | 30 TABLET in 1 BOTTLE (71205-391-30) | Jan 28, 2020 |
| 71205-391-60 | 60 TABLET in 1 BOTTLE (71205-391-60) | Jan 28, 2020 |
| 71205-391-90 | 90 TABLET in 1 BOTTLE (71205-391-90) | Jan 28, 2020 |
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