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Cevimeline Hydrochloride - 60505-3145-5 - (cevimeline hydrochloride)

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Drug Information of Cevimeline Hydrochloride

Product NDC: 60505-3145
Proprietary Name: Cevimeline Hydrochloride
Non Proprietary Name: cevimeline hydrochloride
Active Ingredient(s): 30    mg/1 & nbsp;   cevimeline hydrochloride
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Cevimeline Hydrochloride

Product NDC: 60505-3145
Labeler Name: Apotex Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA091260
Marketing Category: ANDA
Start Marketing Date: 20121008

Package Information of Cevimeline Hydrochloride

Package NDC: 60505-3145-5
Package Description: 500 CAPSULE in 1 BOTTLE (60505-3145-5)

NDC Information of Cevimeline Hydrochloride

NDC Code 60505-3145-5
Proprietary Name Cevimeline Hydrochloride
Package Description 500 CAPSULE in 1 BOTTLE (60505-3145-5)
Product NDC 60505-3145
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name cevimeline hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20121008
Marketing Category Name ANDA
Labeler Name Apotex Corp.
Substance Name CEVIMELINE HYDROCHLORIDE
Strength Number 30
Strength Unit mg/1
Pharmaceutical Classes Cholinergic Muscarinic Agonists [MoA],Cholinergic Receptor Agonist [EPC]

Complete Information of Cevimeline Hydrochloride


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