acyclovir
Generic: acyclovir
Labeler: bryant ranch prepackDrug Facts
Product Profile
Brand Name
acyclovir
Generic Name
acyclovir
Labeler
bryant ranch prepack
Dosage Form
TABLET
Routes
Active Ingredients
acyclovir 800 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
71335-1381
Product ID
71335-1381_ab6cd5b2-f2ba-43b6-99f5-aeedd8a8a069
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA077309
Marketing Start
2006-03-13
Marketing End
2026-12-31
Pharmacologic Class
Established (EPC)
Mechanism of Action
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
713351381
Hyphenated Format
71335-1381
Supplemental Identifiers
RxCUI
UNII
NUI
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
acyclovir (source: ndc)
Generic Name
acyclovir (source: ndc)
Application Number
ANDA077309 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 800 mg/1
Packaging
- 500 TABLET in 1 BOTTLE (71335-1381-0)
- 25 TABLET in 1 BOTTLE (71335-1381-1)
- 35 TABLET in 1 BOTTLE (71335-1381-2)
- 30 TABLET in 1 BOTTLE (71335-1381-3)
- 60 TABLET in 1 BOTTLE (71335-1381-4)
- 50 TABLET in 1 BOTTLE (71335-1381-5)
- 10 TABLET in 1 BOTTLE (71335-1381-6)
- 40 TABLET in 1 BOTTLE (71335-1381-7)
- 21 TABLET in 1 BOTTLE (71335-1381-8)
- 90 TABLET in 1 BOTTLE (71335-1381-9)
Packages (10)
71335-1381-0
500 TABLET in 1 BOTTLE (71335-1381-0)
71335-1381-1
25 TABLET in 1 BOTTLE (71335-1381-1)
71335-1381-2
35 TABLET in 1 BOTTLE (71335-1381-2)
71335-1381-3
30 TABLET in 1 BOTTLE (71335-1381-3)
71335-1381-4
60 TABLET in 1 BOTTLE (71335-1381-4)
71335-1381-5
50 TABLET in 1 BOTTLE (71335-1381-5)
71335-1381-6
10 TABLET in 1 BOTTLE (71335-1381-6)
71335-1381-7
40 TABLET in 1 BOTTLE (71335-1381-7)
71335-1381-8
21 TABLET in 1 BOTTLE (71335-1381-8)
71335-1381-9
90 TABLET in 1 BOTTLE (71335-1381-9)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
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