emtricitabine and tenofovir disoproxil fumarate
Generic: emtricitabine and tenofovir disoproxil fumarate
Labeler: aurobindo pharma limitedDrug Facts
Product Profile
Brand Name
emtricitabine and tenofovir disoproxil fumarate
Generic Name
emtricitabine and tenofovir disoproxil fumarate
Labeler
aurobindo pharma limited
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
emtricitabine 133 mg/1, tenofovir disoproxil fumarate 200 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
59651-166
Product ID
59651-166_a805c27a-1154-4aac-9af8-bbd755be027f
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA211640
Listing Expiration
2026-12-31
Marketing Start
2023-03-09
Pharmacologic Class
Established (EPC)
Mechanism of Action
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
59651166
Hyphenated Format
59651-166
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
emtricitabine and tenofovir disoproxil fumarate (source: ndc)
Generic Name
emtricitabine and tenofovir disoproxil fumarate (source: ndc)
Application Number
ANDA211640 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 133 mg/1
- 200 mg/1
Packaging
- 30 TABLET, FILM COATED in 1 BOTTLE (59651-166-30)
Packages (1)
Ingredients (2)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
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