Acyclovir 71335-0695
Product NDC
71335-0695- Manufacturer
- Bryant Ranch Prepack
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- November 29, 2013
- Listing Expires
- December 31, 2027
- Application
- ANDA203834
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Acyclovir | 800 mg/1 |
Drug Class
Herpes Simplex Virus Nucleoside Analog DNA Polymerase Inhibitor [EPC]Herpes Zoster Virus Nucleoside Analog DNA Polymerase Inhibitor [EPC]Herpesvirus Nucleoside Analog DNA Polymerase Inhibitor [EPC]
Packaging Options(10)
500 TABLET in 1 BOTTLE (71335-0695-0)
25 TABLET in 1 BOTTLE (71335-0695-1)
35 TABLET in 1 BOTTLE (71335-0695-2)
30 TABLET in 1 BOTTLE (71335-0695-3)
60 TABLET in 1 BOTTLE (71335-0695-4)
50 TABLET in 1 BOTTLE (71335-0695-5)
10 TABLET in 1 BOTTLE (71335-0695-6)
40 TABLET in 1 BOTTLE (71335-0695-7)
21 TABLET in 1 BOTTLE (71335-0695-8)
90 TABLET in 1 BOTTLE (71335-0695-9)