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Atropine Sulfate - 24208-825-55 - (Atropine Sulfate)

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Drug Information of Atropine Sulfate

Product NDC: 24208-825
Proprietary Name: Atropine Sulfate
Non Proprietary Name: Atropine Sulfate
Active Ingredient(s): 10    mg/g & nbsp;   Atropine Sulfate
Administration Route(s): OPHTHALMIC
Dosage Form(s): OINTMENT
Coding System: National Drug Codes(NDC)

Labeler Information of Atropine Sulfate

Product NDC: 24208-825
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: 24208-825-55
Package Description: 1 TUBE in 1 CARTON (24208-825-55) > 3.5 g in 1 TUBE

NDC Information of Atropine Sulfate

NDC Code 24208-825-55
Proprietary Name Atropine Sulfate
Package Description 1 TUBE in 1 CARTON (24208-825-55) > 3.5 g in 1 TUBE
Product NDC 24208-825
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Atropine Sulfate
Dosage Form Name OINTMENT
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/g
Pharmaceutical Classes Anticholinergic [EPC],Cholinergic Antagonists [MoA],Cholinergic Muscarinic Antagonist [EPC],Cholinergic Muscarinic Antagonists [MoA]

Complete Information of Atropine Sulfate


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