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Pilocarpine Hydrochloride - 54868-5436-2 - (Pilocarpine Hydrochloride)

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Drug Information of Pilocarpine Hydrochloride

Product NDC: 54868-5436
Proprietary Name: Pilocarpine Hydrochloride
Non Proprietary Name: Pilocarpine Hydrochloride
Active Ingredient(s): 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: 54868-5436
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077220
Marketing Category: ANDA
Start Marketing Date: 20110721

Package Information of Pilocarpine Hydrochloride

Package NDC: 54868-5436-2
Package Description: 100 TABLET, FILM COATED in 1 BOTTLE (54868-5436-2)

NDC Information of Pilocarpine Hydrochloride

NDC Code 54868-5436-2
Proprietary Name Pilocarpine Hydrochloride
Package Description 100 TABLET, FILM COATED in 1 BOTTLE (54868-5436-2)
Product NDC 54868-5436
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Pilocarpine Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20110721
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name PILOCARPINE HYDROCHLORIDE
Strength Number 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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