X (BENAZEPRIL HCL) POWDER [AX PHARMACEUTICAL CORP]

X (BENAZEPRIL HCL) POWDER [AX PHARMACEUTICAL CORP]
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NDC	62157-395-01
Set ID	dc39a7c3-2eb7-4587-a1e2-c4559ea24184
Category	BULK INGREDIENT
Packager	AX Pharmaceutical Corp
Generic Name
Product Class	Angiotensin Converting Enzyme Inhibitor
Product Number
Application Number

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PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

X
benazepril hcl powder

Product Information
Product Type	BULK INGREDIENT	Item Code (Source)	NDC:62157-395
Route of Administration	NOT APPLICABLE

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
BENAZEPRIL HYDROCHLORIDE (UNII: N1SN99T69T) (BENAZEPRILAT - UNII:JRM708L703)	BENAZEPRIL HYDROCHLORIDE	49.5 g in 50 g

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)

Product Characteristics
Color	white	Score
Shape		Size
Flavor		Imprint Code
Contains

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:62157-395-01	50 g in 1 JAR	03/01/2017

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
bulk ingredient for animal drug compounding		03/01/2017

Labeler - AX Pharmaceutical Corp (202924858)

Name	Address	ID/FEI	Business Operations
Establishment
AX Pharmaceutical Corp		202924858	pack(62157-395) , relabel(62157-395)

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