enalaprilat

Generic: enalaprilat

Labeler: hikma pharmaceuticals usa inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name enalaprilat
Generic Name enalaprilat
Labeler hikma pharmaceuticals usa inc.
Dosage Form INJECTION
Routes
INTRAVENOUS
Active Ingredients

enalaprilat dihydrate 2.5 mg/2mL

Manufacturer
Hikma Pharmaceuticals USA Inc.

Identifiers & Regulatory

Product NDC 0143-9786
Product ID 0143-9786_bde8c35d-1cf2-42ea-a2a7-c4eb165e6d0d
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078687
Listing Expiration 2026-12-31
Marketing Start 2008-12-23

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 01439786
Hyphenated Format 0143-9786

Supplemental Identifiers

RxCUI
1729200 1729205
UNII
GV0O7ES0R3

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 enalaprilat (source: ndc)
Generic Name enalaprilat (source: ndc)
Application Number ANDA078687 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 2.5 mg/2mL
source: ndc
Packaging
  • 10 VIAL in 1 CARTON (0143-9786-10) / 2 mL in 1 VIAL (0143-9786-01)
source: ndc

Packages (1)

0143-9786-10 10 VIAL in 1 CARTON (0143-9786-10) / 2 mL in 1 VIAL (0143-9786-01)

Ingredients (1)

enalaprilat dihydrate (2.5 mg/2mL)

Linked Drug Pages (1)

Enalaprilat ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "bde8c35d-1cf2-42ea-a2a7-c4eb165e6d0d", "openfda": {"unii": ["GV0O7ES0R3"], "rxcui": ["1729200", "1729205"], "spl_set_id": ["eabae489-e254-4987-ab90-7cda20a6f856"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 CARTON (0143-9786-10)  / 2 mL in 1 VIAL (0143-9786-01)", "package_ndc": "0143-9786-10", "marketing_start_date": "20081223"}], "brand_name": "Enalaprilat", "product_id": "0143-9786_bde8c35d-1cf2-42ea-a2a7-c4eb165e6d0d", "dosage_form": "INJECTION", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]", "Decreased Blood Pressure [PE]"], "product_ndc": "0143-9786", "generic_name": "enalaprilat", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Enalaprilat", "active_ingredients": [{"name": "ENALAPRILAT DIHYDRATE", "strength": "2.5 mg/2mL"}], "application_number": "ANDA078687", "marketing_category": "ANDA", "marketing_start_date": "20081223", "listing_expiration_date": "20261231"}