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Pilocarpine Hydrochloride - 21695-601-90 - (Pilocarpine Hydrochloride)

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Drug Information of Pilocarpine Hydrochloride

Product NDC: 21695-601
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: 21695-601
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077248
Marketing Category: ANDA
Start Marketing Date: 20060331

Package Information of Pilocarpine Hydrochloride

Package NDC: 21695-601-90
Package Description: 90 TABLET in 1 BOTTLE (21695-601-90)

NDC Information of Pilocarpine Hydrochloride

NDC Code 21695-601-90
Proprietary Name Pilocarpine Hydrochloride
Package Description 90 TABLET in 1 BOTTLE (21695-601-90)
Product NDC 21695-601
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Pilocarpine Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20060331
Marketing Category Name ANDA
Labeler Name Rebel Distributors Corp
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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