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Pilocarpine Hydrochloride - 0054-0056-25 - (Pilocarpine Hydrochloride)

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Drug Information of Pilocarpine Hydrochloride

Product NDC: 0054-0056
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
Coding System: National Drug Codes(NDC)

Labeler Information of Pilocarpine Hydrochloride

Product NDC: 0054-0056
Labeler Name: Roxane Laboratories, Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076963
Marketing Category: ANDA
Start Marketing Date: 20041222

Package Information of Pilocarpine Hydrochloride

Package NDC: 0054-0056-25
Package Description: 100 TABLET in 1 BOTTLE, PLASTIC (0054-0056-25)

NDC Information of Pilocarpine Hydrochloride

NDC Code 0054-0056-25
Proprietary Name Pilocarpine Hydrochloride
Package Description 100 TABLET in 1 BOTTLE, PLASTIC (0054-0056-25)
Product NDC 0054-0056
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Pilocarpine Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20041222
Marketing Category Name ANDA
Labeler Name Roxane Laboratories, 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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