NDC 51655-679 – Acyclovir
Acyclovir 800 mg/1 · Tablet · Oral
Product NDC51655-679
Product details
- Brand name
- Acyclovir
- Generic name
- Acyclovir
- Labeler
- Northwind Health Company, LLC
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA203834
- Marketed since
- February 15, 2023
- Listing expires
- December 31, 2027
- 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 (3)
| Package NDC | Description | Since |
|---|---|---|
| 51655-679-35 | 35 TABLET in 1 BOTTLE, PLASTIC (51655-679-35) | Mar 2, 2023 |
| 51655-679-51 | 40 TABLET in 1 BOTTLE, PLASTIC (51655-679-51) | Feb 15, 2023 |
| 51655-679-52 | 30 TABLET in 1 BOTTLE, PLASTIC (51655-679-52) | Jun 2, 2023 |
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