58118-2271 NDC - AMLODIPINE BESYLATE AND BENAZEPRIL HYDROCHLORIDE ()

Drug Information

Field Name	Field Value
Labeler Name:	Clinical Solutions Wholesale
Product Type:
FDA Application Number:	ANDA020364
Marketing Category:	ANDA
Start Marketing Date:	3/3/1995
End Marketing Date:	6/22/2017

No.	Package Code	Package Description
1	58118-2271-0	1 CAPSULE in 1 PACKET (58118-2271-0)
2	58118-2271-3	30 CAPSULE in 1 BOTTLE, PLASTIC (58118-2271-3)
3	58118-2271-8	30 CAPSULE in 1 BLISTER PACK (58118-2271-8)
4	58118-2271-9	90 CAPSULE in 1 BOTTLE, PLASTIC (58118-2271-9)

Field Name	Field Value	Definition
PRODUCT NDC	58118-2271	The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PROPRIETARY NAME	Amlodipine Besylate and Benazepril Hydrochloride	The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE	3/3/1995	The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
END MARKETING DATE	6/22/2017	Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
MARKETING CATEGORY NAME	ANDA	The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
APPLICATION NUMBER	ANDA020364	The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
LABELER NAME	Clinical Solutions Wholesale	The translation of the dosage form Code submitted by the firm.