enalaprilat
Generic: enalaprilat
Labeler: dr. reddys laboratories incDrug Facts
Product Profile
Brand Name
enalaprilat
Generic Name
enalaprilat
Labeler
dr. reddys laboratories inc
Dosage Form
INJECTION
Routes
Active Ingredients
enalaprilat 2.5 mg/2mL
Manufacturer
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
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
43598169
Hyphenated Format
43598-169
Supplemental Identifiers
RxCUI
UPC
UNII
Packaging Origin
Original Packager
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
source: ndc
Resolved Composition
Strengths
- 2.5 mg/2mL
Packaging
- 10 VIAL in 1 CARTON (43598-169-58) / 2 mL in 1 VIAL (43598-169-11)
Packages (1)
Ingredients (1)
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"}