enalapril maleate

Generic: enalapril maleate

Labeler: taro pharmaceuticals u.s.a., inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name enalapril maleate
Generic Name enalapril maleate
Labeler taro pharmaceuticals u.s.a., inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

enalapril maleate 10 mg/1

Manufacturer
Taro Pharmaceuticals U.S.A., Inc.

Identifiers & Regulatory

Product NDC 51672-4245
Product ID 51672-4245_e64450c0-8dde-4920-9bf9-c714e09e1566
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA075657
Listing Expiration 2026-12-31
Marketing Start 2001-01-23

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 516724245
Hyphenated Format 51672-4245

Supplemental Identifiers

RxCUI
858804 858810 858813 858817
UPC
0351672403812 0351672404017 0351672403713 0351672403911
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 ANDA075657 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (51672-4245-1)
  • 1000 TABLET in 1 BOTTLE (51672-4245-3)
source: ndc

Packages (2)

51672-4245-1 100 TABLET in 1 BOTTLE (51672-4245-1) 51672-4245-3 1000 TABLET in 1 BOTTLE (51672-4245-3)

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": "e64450c0-8dde-4920-9bf9-c714e09e1566", "openfda": {"upc": ["0351672403812", "0351672404017", "0351672403713", "0351672403911"], "unii": ["9O25354EPJ"], "rxcui": ["858804", "858810", "858813", "858817"], "spl_set_id": ["f103b9f9-e081-419d-a2d8-b86acda834dd"], "manufacturer_name": ["Taro Pharmaceuticals U.S.A., Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (51672-4245-1)", "package_ndc": "51672-4245-1", "marketing_start_date": "20230717"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (51672-4245-3)", "package_ndc": "51672-4245-3", "marketing_start_date": "20230717"}], "brand_name": "Enalapril Maleate", "product_id": "51672-4245_e64450c0-8dde-4920-9bf9-c714e09e1566", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]", "Decreased Blood Pressure [PE]"], "product_ndc": "51672-4245", "generic_name": "Enalapril Maleate", "labeler_name": "Taro Pharmaceuticals U.S.A., Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Enalapril Maleate", "active_ingredients": [{"name": "ENALAPRIL MALEATE", "strength": "10 mg/1"}], "application_number": "ANDA075657", "marketing_category": "ANDA", "marketing_start_date": "20010123", "listing_expiration_date": "20261231"}