enalapril maleate

Generic: enalapril maleate

Labeler: solco healthcare us, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name enalapril maleate
Generic Name enalapril maleate
Labeler solco healthcare us, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

enalapril maleate 10 mg/1

Manufacturer
Solco Healthcare US, LLC

Identifiers & Regulatory

Product NDC 43547-547
Product ID 43547-547_c3c8f70a-800d-40f1-8f11-0cc49c51d67c
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA213273
Listing Expiration 2026-12-31
Marketing Start 2022-07-31

Pharmacologic Class

Classes
angiotensin converting enzyme inhibitor [epc] angiotensin-converting enzyme inhibitors [moa] decreased blood pressure [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 43547547
Hyphenated Format 43547-547

Supplemental Identifiers

RxCUI
858804 858810 858813 858817
UPC
0343547548100 0343547547103 0343547545109 0343547546106
UNII
9O25354EPJ

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 (source: ndc)
Generic Name enalapril maleate (source: ndc)
Application Number ANDA213273 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (43547-547-03)
  • 90 TABLET in 1 BOTTLE (43547-547-09)
  • 100 TABLET in 1 BOTTLE (43547-547-10)
  • 1000 TABLET in 1 BOTTLE (43547-547-11)
  • 500 TABLET in 1 BOTTLE (43547-547-50)
source: ndc

Packages (5)

43547-547-03 30 TABLET in 1 BOTTLE (43547-547-03) 43547-547-09 90 TABLET in 1 BOTTLE (43547-547-09) 43547-547-10 100 TABLET in 1 BOTTLE (43547-547-10) 43547-547-11 1000 TABLET in 1 BOTTLE (43547-547-11) 43547-547-50 500 TABLET in 1 BOTTLE (43547-547-50)

Ingredients (1)

enalapril maleate (10 mg/1)

Linked Drug Pages (1)

Enalapril Maleate ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "c3c8f70a-800d-40f1-8f11-0cc49c51d67c", "openfda": {"upc": ["0343547548100", "0343547547103", "0343547545109", "0343547546106"], "unii": ["9O25354EPJ"], "rxcui": ["858804", "858810", "858813", "858817"], "spl_set_id": ["0c829189-fba2-48f8-a23f-d5471a0345f6"], "manufacturer_name": ["Solco Healthcare US, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (43547-547-03)", "package_ndc": "43547-547-03", "marketing_start_date": "20220731"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (43547-547-09)", "package_ndc": "43547-547-09", "marketing_start_date": "20220731"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (43547-547-10)", "package_ndc": "43547-547-10", "marketing_start_date": "20220731"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (43547-547-11)", "package_ndc": "43547-547-11", "marketing_start_date": "20220731"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (43547-547-50)", "package_ndc": "43547-547-50", "marketing_start_date": "20220731"}], "brand_name": "Enalapril Maleate", "product_id": "43547-547_c3c8f70a-800d-40f1-8f11-0cc49c51d67c", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]", "Decreased Blood Pressure [PE]"], "product_ndc": "43547-547", "generic_name": "Enalapril Maleate", "labeler_name": "Solco Healthcare US, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Enalapril Maleate", "active_ingredients": [{"name": "ENALAPRIL MALEATE", "strength": "10 mg/1"}], "application_number": "ANDA213273", "marketing_category": "ANDA", "marketing_start_date": "20220731", "listing_expiration_date": "20261231"}