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Pilocarpine hydrochloride - 0228-2837-11 - (Pilocarpine hydrochloride)

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Drug Information of Pilocarpine hydrochloride

Product NDC: 0228-2837
Proprietary Name: Pilocarpine hydrochloride
Non Proprietary Name: Pilocarpine hydrochloride
Active Ingredient(s): 7.5    mg/1 & nbsp;   Pilocarpine hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Pilocarpine hydrochloride

Product NDC: 0228-2837
Labeler Name: Actavis Elizabeth LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020237
Marketing Category: NDA
Start Marketing Date: 20110913

Package Information of Pilocarpine hydrochloride

Package NDC: 0228-2837-11
Package Description: 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0228-2837-11)

NDC Information of Pilocarpine hydrochloride

NDC Code 0228-2837-11
Proprietary Name Pilocarpine hydrochloride
Package Description 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0228-2837-11)
Product NDC 0228-2837
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Pilocarpine hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20110913
Marketing Category Name NDA
Labeler Name Actavis Elizabeth LLC
Substance Name PILOCARPINE HYDROCHLORIDE
Strength Number 7.5
Strength Unit mg/1
Pharmaceutical Classes Cholinergic Agonists [MoA],Cholinergic Muscarinic Agonists [MoA],Cholinergic Receptor Agonist [EPC]

Complete Information of Pilocarpine hydrochloride


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