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
72162-1724
Product ID
72162-1724_a45392d2-5725-47dc-a6c5-50a98f93031a
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
721621724
Hyphenated Format
72162-1724
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
- 40 TABLET in 1 BOTTLE (72162-1724-0)
- 21 TABLET in 1 BOTTLE (72162-1724-1)
- 25 TABLET in 1 BOTTLE (72162-1724-2)
- 30 TABLET in 1 BOTTLE (72162-1724-3)
- 35 TABLET in 1 BOTTLE (72162-1724-4)
- 500 TABLET in 1 BOTTLE (72162-1724-5)
- 60 TABLET in 1 BOTTLE (72162-1724-6)
- 50 TABLET in 1 BOTTLE (72162-1724-7)
- 10 TABLET in 1 BOTTLE (72162-1724-8)
- 90 TABLET in 1 BOTTLE (72162-1724-9)
Packages (10)
72162-1724-0
40 TABLET in 1 BOTTLE (72162-1724-0)
72162-1724-1
21 TABLET in 1 BOTTLE (72162-1724-1)
72162-1724-2
25 TABLET in 1 BOTTLE (72162-1724-2)
72162-1724-3
30 TABLET in 1 BOTTLE (72162-1724-3)
72162-1724-4
35 TABLET in 1 BOTTLE (72162-1724-4)
72162-1724-5
500 TABLET in 1 BOTTLE (72162-1724-5)
72162-1724-6
60 TABLET in 1 BOTTLE (72162-1724-6)
72162-1724-7
50 TABLET in 1 BOTTLE (72162-1724-7)
72162-1724-8
10 TABLET in 1 BOTTLE (72162-1724-8)
72162-1724-9
90 TABLET in 1 BOTTLE (72162-1724-9)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
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