NDC 0615-8089

BENZTROPINE MESYLATE

Benztropine Mesylate

BENZTROPINE MESYLATE is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Ncs Healthcare Of Ky, Inc Dba Vangard Labs. The primary component is Benztropine Mesylate.

Product ID0615-8089_1a17a9d8-e17e-4ca3-a903-07d700a4a3a0
NDC0615-8089
Product TypeHuman Prescription Drug
Proprietary NameBENZTROPINE MESYLATE
Generic NameBenztropine Mesylate
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2012-11-28
Marketing CategoryANDA / ANDA
Application NumberANDA090168
Labeler NameNCS HealthCare of KY, Inc dba Vangard Labs
Substance NameBENZTROPINE MESYLATE
Active Ingredient Strength1 mg/1
Pharm ClassesAnticholinergic [EPC],Antihistamine [EPC],Cholinergic Antagonists [MoA],Histamine Receptor Antagonists [MoA]
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 0615-8089-39

30 TABLET in 1 BLISTER PACK (0615-8089-39)
Marketing Start Date2016-05-15
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 0615-8089-39 [00615808939]

BENZTROPINE MESYLATE TABLET
Marketing CategoryANDA
Application NumberANDA090168
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2016-05-15
Marketing End Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
BENZTROPINE MESYLATE1 mg/1

OpenFDA Data

SPL SET ID:c1889263-a3b0-4bb4-be44-a855d3a16898
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 885219
  • 885213
  • Pharmacological Class

    • Anticholinergic [EPC]
    • Antihistamine [EPC]
    • Cholinergic Antagonists [MoA]
    • Histamine Receptor Antagonists [MoA]