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Atropine Sulfate - 0409-4911-34 - (ATROPINE SULFATE)

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Drug Information of Atropine Sulfate

Product NDC: 0409-4911
Proprietary Name: Atropine Sulfate
Non Proprietary Name: ATROPINE SULFATE
Active Ingredient(s): .1    mg/mL & nbsp;   ATROPINE SULFATE
Administration Route(s): INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Atropine Sulfate

Product NDC: 0409-4911
Labeler Name: Hospira, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20051025

Package Information of Atropine Sulfate

Package NDC: 0409-4911-34
Package Description: 1 SYRINGE in 1 CARTON (0409-4911-34) > 10 mL in 1 SYRINGE

NDC Information of Atropine Sulfate

NDC Code 0409-4911-34
Proprietary Name Atropine Sulfate
Package Description 1 SYRINGE in 1 CARTON (0409-4911-34) > 10 mL in 1 SYRINGE
Product NDC 0409-4911
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ATROPINE SULFATE
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS
Start Marketing Date 20051025
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name Hospira, Inc.
Substance Name ATROPINE SULFATE
Strength Number .1
Strength Unit mg/mL
Pharmaceutical Classes Anticholinergic [EPC],Cholinergic Antagonists [MoA],Cholinergic Muscarinic Antagonist [EPC],Cholinergic Muscarinic Antagonists [MoA]

Complete Information of Atropine Sulfate


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