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Atropine Sulfate - 0409-9630-05 - (ATROPINE SULFATE)

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Drug Information of Atropine Sulfate

Product NDC: 0409-9630
Proprietary Name: Atropine Sulfate
Non Proprietary Name: ATROPINE SULFATE
Active Ingredient(s): .05    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: 0409-9630
Labeler Name: Hospira, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021146
Marketing Category: NDA
Start Marketing Date: 20110629

Package Information of Atropine Sulfate

Package NDC: 0409-9630-05
Package Description: 10 CARTON in 1 CONTAINER (0409-9630-05) > 1 SYRINGE, PLASTIC in 1 CARTON > 5 mL in 1 SYRINGE, PLASTIC

NDC Information of Atropine Sulfate

NDC Code 0409-9630-05
Proprietary Name Atropine Sulfate
Package Description 10 CARTON in 1 CONTAINER (0409-9630-05) > 1 SYRINGE, PLASTIC in 1 CARTON > 5 mL in 1 SYRINGE, PLASTIC
Product NDC 0409-9630
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ATROPINE SULFATE
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS
Start Marketing Date 20110629
Marketing Category Name NDA
Labeler Name Hospira, Inc.
Substance Name ATROPINE SULFATE
Strength Number .05
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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