enalapril maleate and hydrochlorothiazide

Generic: enalapril maleate and hydrochlorothiazide

Labeler: dr. reddy's laboratories limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name enalapril maleate and hydrochlorothiazide
Generic Name enalapril maleate and hydrochlorothiazide
Labeler dr. reddy's laboratories limited
Dosage Form TABLET
Routes
ORAL
Active Ingredients

enalapril maleate 5 mg/1, hydrochlorothiazide 12.5 mg/1

Manufacturer
Dr. Reddy's Laboratories Limited

Identifiers & Regulatory

Product NDC 55111-133
Product ID 55111-133_8b3e7cd9-3a3d-7b47-d751-09ab6cee3d1b
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA075909
Listing Expiration 2026-12-31
Marketing Start 2001-10-15

Pharmacologic Class

Established (EPC)
thiazide diuretic [epc]
Chemical Structure
thiazides [cs]
Physiologic Effect
increased diuresis [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 55111133
Hyphenated Format 55111-133

Supplemental Identifiers

RxCUI
858824 858828
UNII
0J48LPH2TH 9O25354EPJ
NUI
N0000175359 N0000175419 M0471776

Packaging Origin

Original Packager
true

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 enalapril maleate and hydrochlorothiazide (source: ndc)
Generic Name enalapril maleate and hydrochlorothiazide (source: ndc)
Application Number ANDA075909 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
  • 12.5 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (55111-133-01)
  • 1000 TABLET in 1 BOTTLE (55111-133-10)
source: ndc

Packages (2)

55111-133-01 100 TABLET in 1 BOTTLE (55111-133-01) 55111-133-10 1000 TABLET in 1 BOTTLE (55111-133-10)

Ingredients (2)

enalapril maleate (5 mg/1) hydrochlorothiazide (12.5 mg/1)

Linked Drug Pages (1)

Enalapril maleate and hydrochlorothiazide ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "8b3e7cd9-3a3d-7b47-d751-09ab6cee3d1b", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "unii": ["0J48LPH2TH", "9O25354EPJ"], "rxcui": ["858824", "858828"], "spl_set_id": ["ed4a55a6-cd6a-c74a-cb93-4b45641691a0"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["Dr. Reddy's Laboratories Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (55111-133-01)", "package_ndc": "55111-133-01", "marketing_start_date": "20011015"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (55111-133-10)", "package_ndc": "55111-133-10", "marketing_start_date": "20011015"}], "brand_name": "Enalapril maleate and hydrochlorothiazide", "product_id": "55111-133_8b3e7cd9-3a3d-7b47-d751-09ab6cee3d1b", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]", "Decreased Blood Pressure [PE]", "Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "55111-133", "generic_name": "Enalapril maleate and hydrochlorothiazide", "labeler_name": "Dr. Reddy's Laboratories Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Enalapril maleate and hydrochlorothiazide", "active_ingredients": [{"name": "ENALAPRIL MALEATE", "strength": "5 mg/1"}, {"name": "HYDROCHLOROTHIAZIDE", "strength": "12.5 mg/1"}], "application_number": "ANDA075909", "marketing_category": "ANDA", "marketing_start_date": "20011015", "listing_expiration_date": "20261231"}