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Atropine Sulfate - 24208-750-60 - (Atropine Sulfate)

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Drug Information of Atropine Sulfate

Product NDC: 24208-750
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
Coding System: National Drug Codes(NDC)

Labeler Information of Atropine Sulfate

Product NDC: 24208-750
Labeler Name: Bausch & Lomb Incorporated
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 19900930

Package Information of Atropine Sulfate

Package NDC: 24208-750-60
Package Description: 1 BOTTLE, DROPPER in 1 CARTON (24208-750-60) > 5 mL in 1 BOTTLE, DROPPER

NDC Information of Atropine Sulfate

NDC Code 24208-750-60
Proprietary Name Atropine Sulfate
Package Description 1 BOTTLE, DROPPER in 1 CARTON (24208-750-60) > 5 mL in 1 BOTTLE, DROPPER
Product NDC 24208-750
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Atropine Sulfate
Dosage Form Name SOLUTION
Route Name OPHTHALMIC
Start Marketing Date 19900930
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name Bausch & Lomb Incorporated
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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