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Atropine Sulfate - 17478-214-12 - (Atropine Sulfate)

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Drug Information of Atropine Sulfate

Product NDC: 17478-214
Proprietary Name: Atropine Sulfate
Non Proprietary Name: Atropine Sulfate
Active Ingredient(s): 10    mg/mL & nbsp;   Atropine Sulfate
Administration Route(s): OPHTHALMIC
Dosage Form(s): SOLUTION/ DROPS
Coding System: National Drug Codes(NDC)

Labeler Information of Atropine Sulfate

Product NDC: 17478-214
Labeler Name: Akorn, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 19950601

Package Information of Atropine Sulfate

Package NDC: 17478-214-12
Package Description: 1 BOTTLE, DROPPER in 1 CARTON (17478-214-12) > 15 mL in 1 BOTTLE, DROPPER

NDC Information of Atropine Sulfate

NDC Code 17478-214-12
Proprietary Name Atropine Sulfate
Package Description 1 BOTTLE, DROPPER in 1 CARTON (17478-214-12) > 15 mL in 1 BOTTLE, DROPPER
Product NDC 17478-214
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Atropine Sulfate
Dosage Form Name SOLUTION/ DROPS
Route Name OPHTHALMIC
Start Marketing Date 19950601
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name Akorn, Inc.
Substance Name ATROPINE SULFATE
Strength Number 10
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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