59762-3148 NDC - BENAZEPRIL HYDROCHLORIDE ()

Drug Information

  • Product NDC: 59762-3148
  • Proprietary Name: Benazepril Hydrochloride
  • Non Proprietary Name:
  • Active Ingredient(s):
  • Administration Route(s):
  • Dosage Form(s):

Labeler Information

Field Name Field Value
Labeler Name: Greenstone LLC
Product Type:
FDA Application Number: ANDA078212
Marketing Category: ANDA
Start Marketing Date:5/22/2008
End Marketing Date:3/31/2013

Package Information

No. Package Code Package Description Billing Unit
159762-3148-190 TABLET, FILM COATED in 1 BOTTLE (59762-3148-1)EA
259762-3148-2100 TABLET, FILM COATED in 1 BOTTLE (59762-3148-2)EA

NDC Record

Field Name Field Value Definition
PRODUCT NDC59762-3148Name of Company corresponding to the labeler code segment of the Product NDC.
PROPRIETARY NAMEBenazepril HydrochlorideThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE5/22/2008Name of Company corresponding to the labeler code segment of the Product NDC.
END MARKETING DATE3/31/2013This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.
MARKETING CATEGORY NAMEANDAAn active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
APPLICATION NUMBERANDA078212This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.
LABELER NAMEGreenstone LLCName of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 11/21/2025

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