NDC 61703-237-44 - Enalaprilat

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC: 61703-237
Requested NDC: 61703-237-44
Package NDCs from labels: 61703-237-44, 61703-237-16
Manufacturer: Mayne Pharma (USA) Inc.
Effective date: 2007-03-16
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Enalaprilat - Mayne Pharma (USA) Inc.	Mayne Pharma (USA) Inc.	2007-03-16	Human Prescription Drug Label

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
61703-237-16	Enalaprilat	2 mL in 1 VIAL	INJECTION, SOLUTION	2		1
61703-237-44	Enalaprilat	1 mL in 1 VIAL	INJECTION, SOLUTION	1		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
61703-237	ENALAPRILAT (ENALAPRILAT) INJECTION, SOLUTION [MAYNE PHARMA (USA) INC.]	1	2 package rows	20080313_895c7f90-2c53-43c3-ae4d-31d858e11eff.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
enalaprilat	ACTIVE INGREDIENT	GV0O7ES0R3	ENALAPRILAT (ENALAPRILAT) INJECTION, SOLUTION [MAYNE PHARMA (USA) INC.]	1
enalaprilat	ACTIVE MOIETY	GV0O7ES0R3	ENALAPRILAT (ENALAPRILAT) INJECTION, SOLUTION [MAYNE PHARMA (USA) INC.]	1
benzyl alcohol	INACTIVE INGREDIENT	LKG8494WBH	ENALAPRILAT (ENALAPRILAT) INJECTION, SOLUTION [MAYNE PHARMA (USA) INC.]	1
sodium chloride	INACTIVE INGREDIENT	451W47IQ8X	ENALAPRILAT (ENALAPRILAT) INJECTION, SOLUTION [MAYNE PHARMA (USA) INC.]	1
sodium hydroxide	INACTIVE INGREDIENT	55X04QC32I	ENALAPRILAT (ENALAPRILAT) INJECTION, SOLUTION [MAYNE PHARMA (USA) INC.]	1
Water	INACTIVE INGREDIENT	059QF0KO0R	ENALAPRILAT (ENALAPRILAT) INJECTION, SOLUTION [MAYNE PHARMA (USA) INC.]	1

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 2 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Enalaprilat	ENALAPRILAT	Dr. Reddys Laboratories Inc	5d398da1-020c-ccb1-a775-ce8e0b29d621	2024-06-07	Boxed warning, Warnings, Adverse reactions	Exact identifier rxcui: 1729205
Enalaprilat	ENALAPRILAT	Hikma Pharmaceuticals USA Inc.	eabae489-e254-4987-ab90-7cda20a6f856	2024-01-04	Boxed warning, Warnings, Adverse reactions	Exact identifier rxcui: 1729205

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.