losartan potassium
Generic: losartan potassium
Labeler: bryant ranch prepackDrug Facts
Product Profile
Brand Name
losartan potassium
Generic Name
losartan potassium
Labeler
bryant ranch prepack
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
losartan potassium 100 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
71335-2083
Product ID
71335-2083_99e2c90f-c40d-47cd-aa57-b0d0aca07bda
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA091497
Listing Expiration
2026-12-31
Marketing Start
2014-07-30
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
713352083
Hyphenated Format
71335-2083
Supplemental Identifiers
RxCUI
UNII
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
losartan potassium (source: ndc)
Generic Name
losartan potassium (source: ndc)
Application Number
ANDA091497 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 100 mg/1
Packaging
- 30 TABLET, FILM COATED in 1 BOTTLE (71335-2083-1)
- 60 TABLET, FILM COATED in 1 BOTTLE (71335-2083-2)
- 90 TABLET, FILM COATED in 1 BOTTLE (71335-2083-3)
- 120 TABLET, FILM COATED in 1 BOTTLE (71335-2083-4)
- 100 TABLET, FILM COATED in 1 BOTTLE (71335-2083-5)
- 28 TABLET, FILM COATED in 1 BOTTLE (71335-2083-6)
- 10 TABLET, FILM COATED in 1 BOTTLE (71335-2083-7)
- 180 TABLET, FILM COATED in 1 BOTTLE (71335-2083-8)
Packages (8)
71335-2083-1
30 TABLET, FILM COATED in 1 BOTTLE (71335-2083-1)
71335-2083-2
60 TABLET, FILM COATED in 1 BOTTLE (71335-2083-2)
71335-2083-3
90 TABLET, FILM COATED in 1 BOTTLE (71335-2083-3)
71335-2083-4
120 TABLET, FILM COATED in 1 BOTTLE (71335-2083-4)
71335-2083-5
100 TABLET, FILM COATED in 1 BOTTLE (71335-2083-5)
71335-2083-6
28 TABLET, FILM COATED in 1 BOTTLE (71335-2083-6)
71335-2083-7
10 TABLET, FILM COATED in 1 BOTTLE (71335-2083-7)
71335-2083-8
180 TABLET, FILM COATED in 1 BOTTLE (71335-2083-8)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
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