ezetimibe and simvastatin
Generic: ezetimibe and simvastatin
Labeler: aurobindo pharma limitedDrug Facts
Product Profile
Brand Name
ezetimibe and simvastatin
Generic Name
ezetimibe and simvastatin
Labeler
aurobindo pharma limited
Dosage Form
TABLET
Routes
Active Ingredients
ezetimibe 10 mg/1, simvastatin 20 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
59651-836
Product ID
59651-836_0d4244dd-a226-4677-a6b2-6a1b5cd88790
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA200082
Listing Expiration
2026-12-31
Marketing Start
2024-03-01
Pharmacologic Class
Established (EPC)
Mechanism of Action
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
59651836
Hyphenated Format
59651-836
Supplemental Identifiers
RxCUI
UNII
NUI
Packaging Origin
Original Packager
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
ezetimibe and simvastatin (source: ndc)
Generic Name
ezetimibe and simvastatin (source: ndc)
Application Number
ANDA200082 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 mg/1
- 20 mg/1
Packaging
- 30 TABLET in 1 BOTTLE (59651-836-30)
- 90 TABLET in 1 BOTTLE (59651-836-90)
Packages (2)
Ingredients (2)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
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