67296-1558 NDC - ATENOLOL ()

Drug Information

  • Product NDC: 67296-1558
  • Proprietary Name: Atenolol
  • Non Proprietary Name:
  • Active Ingredient(s):
  • Administration Route(s):
  • Dosage Form(s):

Labeler Information

Field Name Field Value
Labeler Name: RedPharm Drug, Inc.
Product Type:
FDA Application Number: ANDA076900
Marketing Category: ANDA
Start Marketing Date:10/8/2005

Package Information

No. Package Code Package Description Billing Unit
167296-1558-330 TABLET in 1 BOTTLE (67296-1558-3)

NDC Record

Field Name Field Value Definition
PRODUCT NDC67296-1558The 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 NAMEAtenololIndicates 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.
START MARKETING DATE10/8/2005This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEANDAThe translation of the dosage form Code submitted by the firm.
APPLICATION NUMBERANDA076900The translation of the route code submitted by the firm, indicating route of administration.
LABELER NAMERedPharm Drug, Inc.Name of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 3/6/2026

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