ketoconazole
Generic: ketoconazole
Labeler: bryant ranch prepackDrug Facts
Product Profile
Brand Name
ketoconazole
Generic Name
ketoconazole
Labeler
bryant ranch prepack
Dosage Form
TABLET
Routes
Active Ingredients
ketoconazole 200 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
71335-0439
Product ID
71335-0439_ae8e3f89-1b77-4934-9252-64d9888d13fd
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA075319
Listing Expiration
2026-12-31
Marketing Start
1999-06-15
Pharmacologic Class
Established (EPC)
Mechanism of Action
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
713350439
Hyphenated Format
71335-0439
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
ketoconazole (source: ndc)
Generic Name
ketoconazole (source: ndc)
Application Number
ANDA075319 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 200 mg/1
Packaging
- 10 TABLET in 1 BOTTLE (71335-0439-1)
- 30 TABLET in 1 BOTTLE (71335-0439-2)
- 40 TABLET in 1 BOTTLE (71335-0439-3)
- 60 TABLET in 1 BOTTLE (71335-0439-4)
- 8 TABLET in 1 BOTTLE (71335-0439-5)
- 7 TABLET in 1 BOTTLE (71335-0439-6)
- 14 TABLET in 1 BOTTLE (71335-0439-7)
- 90 TABLET in 1 BOTTLE (71335-0439-8)
Packages (8)
71335-0439-1
10 TABLET in 1 BOTTLE (71335-0439-1)
71335-0439-2
30 TABLET in 1 BOTTLE (71335-0439-2)
71335-0439-3
40 TABLET in 1 BOTTLE (71335-0439-3)
71335-0439-4
60 TABLET in 1 BOTTLE (71335-0439-4)
71335-0439-5
8 TABLET in 1 BOTTLE (71335-0439-5)
71335-0439-6
7 TABLET in 1 BOTTLE (71335-0439-6)
71335-0439-7
14 TABLET in 1 BOTTLE (71335-0439-7)
71335-0439-8
90 TABLET in 1 BOTTLE (71335-0439-8)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
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