Drug Information

Product NDC: 76329-1469

Proprietary Name: Naloxone Hydrochloride

Non Proprietary Name: Naloxone Hydrochloride

Active Ingredient(s):

Administration Route(s): PARENTERAL

Dosage Form(s): INJECTION

Pharmacy Class(es):
  • Opioid Antagonist [EPC];
  • Opioid Antagonists [MoA]

Labeler Information

Labeler Name: International Medication Systems, Limited
FDA Application Number: ANDA072076
Marketing Category: ANDA
Start Marketing Date:4/1/1988

Package Information

No. Package Code Package Description Billing Unit
176329-1469-110 SYRINGE in 1 BOX (76329-1469-1) > 2 mL in 1 SYRINGEML

NDC Record

Field Name Field Value Definition
PRODUCT NDC76329-1469The 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 PRESCRIPTION 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 NAMENaloxone HydrochlorideThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMENaloxone HydrochlorideThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMEINJECTIONThe translation of the dosage form Code submitted by the firm.
ROUTE NAMEPARENTERALThe translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE4/1/1988This 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 NUMBERANDA072076This 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 NAMEInternational Medication Systems, LimitedName of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMENALOXONE HYDROCHLORIDEThis is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.
PHARM CLASSESOpioid Antagonist [EPC],Opioid Antagonists [MoA] 

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This page was last updated on: 7/26/2021