enalapril maleate

Generic: enalapril maleate

Labeler: northstar rxllc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name enalapril maleate
Generic Name enalapril maleate
Labeler northstar rxllc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

enalapril maleate 20 mg/1

Manufacturer
Northstar RxLLC

Identifiers & Regulatory

Product NDC 16714-445
Product ID 16714-445_4bc84994-0116-425c-8dab-ba08b0880b24
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA075459
Listing Expiration 2026-12-31
Marketing Start 2015-08-06

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 16714445
Hyphenated Format 16714-445

Supplemental Identifiers

RxCUI
858804 858810 858813 858817
UPC
0316714445014 0316714443010
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 ANDA075459 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (16714-445-01)
  • 1000 TABLET in 1 BOTTLE (16714-445-02)
source: ndc

Packages (2)

16714-445-01 100 TABLET in 1 BOTTLE (16714-445-01) 16714-445-02 1000 TABLET in 1 BOTTLE (16714-445-02)

Ingredients (1)

enalapril maleate (20 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": "4bc84994-0116-425c-8dab-ba08b0880b24", "openfda": {"upc": ["0316714445014", "0316714443010"], "unii": ["9O25354EPJ"], "rxcui": ["858804", "858810", "858813", "858817"], "spl_set_id": ["e109e7b1-4650-4416-9d89-7c1185d5cf48"], "manufacturer_name": ["Northstar RxLLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (16714-445-01)", "package_ndc": "16714-445-01", "marketing_start_date": "20150806"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (16714-445-02)", "package_ndc": "16714-445-02", "marketing_start_date": "20150806"}], "brand_name": "Enalapril Maleate", "product_id": "16714-445_4bc84994-0116-425c-8dab-ba08b0880b24", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]", "Decreased Blood Pressure [PE]"], "product_ndc": "16714-445", "generic_name": "enalapril maleate", "labeler_name": "Northstar RxLLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Enalapril Maleate", "active_ingredients": [{"name": "ENALAPRIL MALEATE", "strength": "20 mg/1"}], "application_number": "ANDA075459", "marketing_category": "ANDA", "marketing_start_date": "20150806", "listing_expiration_date": "20261231"}