11704-105 NDC - ATROPEN AUTO-INJECTOR (ATROPINE)

Drug Information

Product NDC: 11704-105

Proprietary Name: ATROPEN Auto-Injector

Non Proprietary Name: atropine

Active Ingredient(s):
  • 1 mg/.7mL ATROPINE


Administration Route(s): INTRAMUSCULAR

Dosage Form(s): INJECTION

Pharmacy Class(es):
  • Anticholinergic [EPC];
  • Cholinergic Antagonists [MoA];
  • Cholinergic Muscarinic Antagonist [EPC];
  • Cholinergic Muscarinic Antagonists [MoA]

Labeler Information

Labeler Name: Meridian Medical Technologies, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA017106
Marketing Category: NDA
Start Marketing Date:6/19/2003

Package Information

No. Package Code Package Description Billing Unit
111704-105-01.7 mL in 1 SYRINGE, PLASTIC (11704-105-01)ML

NDC Record

Field Name Field Value Definition
PRODUCT NDC11704-105The 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 NAMEATROPEN Auto-InjectorThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEatropineThe 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 NAMEINTRAMUSCULARThe translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE6/19/2003This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMENDAProduct 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 NUMBERNDA017106This 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 NAMEMeridian Medical Technologies, Inc.Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEATROPINEThis is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.
ACTIVE NUMERATOR STRENGTH1 
ACTIVE INGRED UNITmg/.7mL 
PHARM CLASSESAnticholinergic [EPC],Cholinergic Antagonists [MoA],Cholinergic Muscarinic Antagonist [EPC],Cholinergic Muscarinic Antagonists [MoA] 

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This page was last updated on: 8/16/2019