NDC 71335-0323 – Acyclovir
Acyclovir 400 mg/1 · Tablet · Oral
Product NDC71335-0323
Product details
- Brand name
- Acyclovir
- Generic name
- Acyclovir
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA203834
- Marketed since
- November 29, 2013
- 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 400 mg/1
Package NDC codes (10)
| Package NDC | Description | Since |
|---|---|---|
| 71335-0323-0 | 120 TABLET in 1 BOTTLE (71335-0323-0) | May 2, 2018 |
| 71335-0323-1 | 20 TABLET in 1 BOTTLE (71335-0323-1) | Dec 27, 2021 |
| 71335-0323-2 | 28 TABLET in 1 BOTTLE (71335-0323-2) | Dec 27, 2021 |
| 71335-0323-3 | 30 TABLET in 1 BOTTLE (71335-0323-3) | Mar 20, 2018 |
| 71335-0323-4 | 50 TABLET in 1 BOTTLE (71335-0323-4) | Dec 27, 2021 |
| 71335-0323-5 | 15 TABLET in 1 BOTTLE (71335-0323-5) | Apr 17, 2018 |
| 71335-0323-6 | 60 TABLET in 1 BOTTLE (71335-0323-6) | Jul 29, 2019 |
| 71335-0323-7 | 25 TABLET in 1 BOTTLE (71335-0323-7) | Mar 28, 2018 |
| 71335-0323-8 | 10 TABLET in 1 BOTTLE (71335-0323-8) | Dec 27, 2021 |
| 71335-0323-9 | 40 TABLET in 1 BOTTLE (71335-0323-9) | Dec 27, 2021 |
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