72036-109 NDC - IBUPROFEN

Drug Information

Product NDC: 72036-109

Proprietary Name: Ibuprofen

Non Proprietary Name: Ibuprofen

Active Ingredient(s):
  • 200 mg/1 IBUPROFEN


Administration Route(s): ORAL

Dosage Form(s): TABLET, COATED

Pharmacy Class(es):
  • Anti-Inflammatory Agents;
  • Non-Steroidal [CS];
  • Cyclooxygenase Inhibitors [MoA];
  • Nonsteroidal Anti-inflammatory Drug [EPC]

Labeler Information

Labeler Name: Harris Teeter
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA079174
Marketing Category: ANDA
Start Marketing Date:7/23/2012

Package Information

No. Package Code Package Description Billing Unit
172036-109-011 BOTTLE, PLASTIC in 1 CARTON (72036-109-01) / 24 TABLET, COATED in 1 BOTTLE, PLASTIC
272036-109-021 BOTTLE, PLASTIC in 1 CARTON (72036-109-02) / 50 TABLET, COATED in 1 BOTTLE, PLASTIC
372036-109-031 BOTTLE, PLASTIC in 1 CARTON (72036-109-03) / 100 TABLET, COATED in 1 BOTTLE, PLASTIC
472036-109-05500 TABLET, COATED in 1 BOTTLE, PLASTIC (72036-109-05)
572036-109-08300 TABLET, COATED in 1 BOTTLE, PLASTIC (72036-109-08)

NDC Record

Field Name Field Value Definition
PRODUCT NDC72036-109The 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.
PRODUCT TYPE NAMEHUMAN OTC DRUGIndicates 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 NAMEIbuprofenThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEIbuprofenThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMETABLET, COATEDThe translation of the dosage form Code submitted by the firm.
ROUTE NAMEORALThe translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE7/23/2012This 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 NUMBERANDA079174This 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 NAMEHarris TeeterName of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEIBUPROFENAn 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.
ACTIVE NUMERATOR STRENGTH200 
ACTIVE INGRED UNITmg/1 
PHARM CLASSESAnti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC] 

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This page was last updated on: 2/1/2023