lisinopril and hydrochlorothiazide
Generic: lisinopril and hydrochlorothiazide tablets
Labeler: bryant ranch prepackDrug Facts
Product Profile
Brand Name
lisinopril and hydrochlorothiazide
Generic Name
lisinopril and hydrochlorothiazide tablets
Labeler
bryant ranch prepack
Dosage Form
TABLET
Routes
Active Ingredients
hydrochlorothiazide 25 mg/1, lisinopril 20 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
71335-2091
Product ID
71335-2091_746b1295-24a9-46f9-9032-2d85c0367205
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA076230
Listing Expiration
2026-12-31
Marketing Start
2015-03-12
Pharmacologic Class
Established (EPC)
Chemical Structure
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
713352091
Hyphenated Format
71335-2091
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 tablets (source: ndc)
Application Number
ANDA076230 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 25 mg/1
- 20 mg/1
Packaging
- 30 TABLET in 1 BOTTLE (71335-2091-1)
- 60 TABLET in 1 BOTTLE (71335-2091-2)
- 90 TABLET in 1 BOTTLE (71335-2091-3)
- 120 TABLET in 1 BOTTLE (71335-2091-4)
- 100 TABLET in 1 BOTTLE (71335-2091-5)
- 180 TABLET in 1 BOTTLE (71335-2091-6)
Packages (6)
71335-2091-1
30 TABLET in 1 BOTTLE (71335-2091-1)
71335-2091-2
60 TABLET in 1 BOTTLE (71335-2091-2)
71335-2091-3
90 TABLET in 1 BOTTLE (71335-2091-3)
71335-2091-4
120 TABLET in 1 BOTTLE (71335-2091-4)
71335-2091-5
100 TABLET in 1 BOTTLE (71335-2091-5)
71335-2091-6
180 TABLET in 1 BOTTLE (71335-2091-6)
Ingredients (2)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
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