lisinopril and hydrochlorothiazide
Generic: lisinopril and hydrochlorothiazide
Labeler: bryant ranch prepackDrug Facts
Product Profile
Brand Name
lisinopril and hydrochlorothiazide
Generic Name
lisinopril and hydrochlorothiazide
Labeler
bryant ranch prepack
Dosage Form
TABLET
Routes
Active Ingredients
hydrochlorothiazide 12.5 mg/1, lisinopril 10 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
71335-0479
Product ID
71335-0479_aad9eb2a-fdf1-4bfd-9f5a-d8aed8e643f8
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA077912
Listing Expiration
2026-12-31
Marketing Start
2006-10-04
Pharmacologic Class
Established (EPC)
Chemical Structure
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
713350479
Hyphenated Format
71335-0479
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
lisinopril and hydrochlorothiazide (source: ndc)
Generic Name
lisinopril and hydrochlorothiazide (source: ndc)
Application Number
ANDA077912 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 12.5 mg/1
- 10 mg/1
Packaging
- 90 TABLET in 1 BOTTLE (71335-0479-1)
- 60 TABLET in 1 BOTTLE (71335-0479-2)
- 30 TABLET in 1 BOTTLE (71335-0479-3)
- 100 TABLET in 1 BOTTLE (71335-0479-4)
- 120 TABLET in 1 BOTTLE (71335-0479-5)
Packages (5)
Ingredients (2)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
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