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Atropine Sulfate - 0517-0401-25 - (Atropine Sulfate)

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Drug Information of Atropine Sulfate

Product NDC: 0517-0401
Proprietary Name: Atropine Sulfate
Non Proprietary Name: Atropine Sulfate
Active Ingredient(s): .4    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: 0517-0401
Labeler Name: American Regent, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 19921101

Package Information of Atropine Sulfate

Package NDC: 0517-0401-25
Package Description: 25 VIAL, SINGLE-DOSE in 1 TRAY (0517-0401-25) > 1 mL in 1 VIAL, SINGLE-DOSE

NDC Information of Atropine Sulfate

NDC Code 0517-0401-25
Proprietary Name Atropine Sulfate
Package Description 25 VIAL, SINGLE-DOSE in 1 TRAY (0517-0401-25) > 1 mL in 1 VIAL, SINGLE-DOSE
Product NDC 0517-0401
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Atropine Sulfate
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS
Start Marketing Date 19921101
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name American Regent, Inc.
Substance Name ATROPINE SULFATE
Strength Number .4
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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