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 400 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
71335-1053
Product ID
71335-1053_93537a74-6bc3-4da2-865f-73752bf24e54
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA075382
Listing Expiration
2026-12-31
Marketing Start
2009-10-22
Pharmacologic Class
Established (EPC)
Mechanism of Action
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
713351053
Hyphenated Format
71335-1053
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
ANDA075382 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 400 mg/1
Packaging
- 120 TABLET in 1 BOTTLE (71335-1053-0)
- 20 TABLET in 1 BOTTLE (71335-1053-1)
- 28 TABLET in 1 BOTTLE (71335-1053-2)
- 30 TABLET in 1 BOTTLE (71335-1053-3)
- 50 TABLET in 1 BOTTLE (71335-1053-4)
- 15 TABLET in 1 BOTTLE (71335-1053-5)
- 60 TABLET in 1 BOTTLE (71335-1053-6)
- 25 TABLET in 1 BOTTLE (71335-1053-7)
- 10 TABLET in 1 BOTTLE (71335-1053-8)
- 40 TABLET in 1 BOTTLE (71335-1053-9)
Packages (10)
71335-1053-0
120 TABLET in 1 BOTTLE (71335-1053-0)
71335-1053-1
20 TABLET in 1 BOTTLE (71335-1053-1)
71335-1053-2
28 TABLET in 1 BOTTLE (71335-1053-2)
71335-1053-3
30 TABLET in 1 BOTTLE (71335-1053-3)
71335-1053-4
50 TABLET in 1 BOTTLE (71335-1053-4)
71335-1053-5
15 TABLET in 1 BOTTLE (71335-1053-5)
71335-1053-6
60 TABLET in 1 BOTTLE (71335-1053-6)
71335-1053-7
25 TABLET in 1 BOTTLE (71335-1053-7)
71335-1053-8
10 TABLET in 1 BOTTLE (71335-1053-8)
71335-1053-9
40 TABLET in 1 BOTTLE (71335-1053-9)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
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