enalaprilat

Generic: enalaprilat

Labeler: dr. reddys laboratories inc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name enalaprilat
Generic Name enalaprilat
Labeler dr. reddys laboratories inc
Dosage Form INJECTION
Routes
INTRAVENOUS
Active Ingredients

enalaprilat 2.5 mg/2mL

Manufacturer
Dr. Reddys Laboratories Inc

Identifiers & Regulatory

Product NDC 43598-169
Product ID 43598-169_d20e2c0a-b04d-5e4a-a28b-442e0a77f3b6
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA075578
Listing Expiration 2026-12-31
Marketing Start 2023-06-06

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 43598169
Hyphenated Format 43598-169

Supplemental Identifiers

RxCUI
1729200 1729205
UPC
0343598078113 0343598169118 0343598078588 0343598169583
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 ANDA075578 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 2.5 mg/2mL
source: ndc
Packaging
  • 10 VIAL in 1 CARTON (43598-169-58) / 2 mL in 1 VIAL (43598-169-11)
source: ndc

Packages (1)

Ingredients (1)

enalaprilat (2.5 mg/2mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "d20e2c0a-b04d-5e4a-a28b-442e0a77f3b6", "openfda": {"upc": ["0343598078113", "0343598169118", "0343598078588", "0343598169583"], "unii": ["GV0O7ES0R3"], "rxcui": ["1729200", "1729205"], "spl_set_id": ["5d398da1-020c-ccb1-a775-ce8e0b29d621"], "manufacturer_name": ["Dr. Reddys Laboratories Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 CARTON (43598-169-58)  / 2 mL in 1 VIAL (43598-169-11)", "package_ndc": "43598-169-58", "marketing_start_date": "20230606"}], "brand_name": "Enalaprilat", "product_id": "43598-169_d20e2c0a-b04d-5e4a-a28b-442e0a77f3b6", "dosage_form": "INJECTION", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]", "Decreased Blood Pressure [PE]"], "product_ndc": "43598-169", "generic_name": "enalaprilat", "labeler_name": "Dr. Reddys Laboratories Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Enalaprilat", "active_ingredients": [{"name": "ENALAPRILAT", "strength": "2.5 mg/2mL"}], "application_number": "ANDA075578", "marketing_category": "ANDA", "marketing_start_date": "20230606", "listing_expiration_date": "20261231"}