67296-1156 NDC - AMOXICILLIN ()

Drug Information

  • Product NDC: 67296-1156
  • Proprietary Name: Amoxicillin
  • 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: ANDA065271
Marketing Category: ANDA
Start Marketing Date:11/9/2005

Package Information

No. Package Code Package Description Billing Unit
167296-1156-220 CAPSULE in 1 BOTTLE (67296-1156-2)
267296-1156-330 CAPSULE in 1 BOTTLE (67296-1156-3)
367296-1156-440 CAPSULE in 1 BOTTLE (67296-1156-4)
467296-1156-521 CAPSULE in 1 BOTTLE (67296-1156-5)
567296-1156-660 CAPSULE in 1 BOTTLE (67296-1156-6)
667296-1156-742 CAPSULE in 1 BOTTLE (67296-1156-7)

NDC Record

Field Name Field Value Definition
PRODUCT NDC67296-1156Indicates 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.
PROPRIETARY NAMEAmoxicillinThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE11/9/2005This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEANDAProduct types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
APPLICATION NUMBERANDA065271This 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 NAMERedPharm Drug, Inc.Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

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This page was last updated on: 2/5/2026

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