Benztropine Mesylate

Product NDC
0832-1080
11-digit product format
008321080
Labeler code
0832
Product ID
0832-1080_2711e70f-cc34-4092-b4fc-47e426cef420
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
benztropine mesylate
Dosage form
TABLET
Route
ORAL
Labeler
Upsher-Smith Laboratories, LLC
Application
ANDA040103
Marketing category
ANDA
Marketing start
1996-12-12
Marketing end
0000-00-00
Substance
BENZTROPINE MESYLATE
Active strength
1 mg/1
Pharmacologic classes
Anticholinergic [EPC],Antihistamine [EPC],Cholinergic Antagonists [MoA],Histamine Receptor Antagonists [MoA]
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
2961cf47-535c-c402-c24d-0a9130269674Product name320251121
3f930a8b-cc65-fba9-e4ca-58b6abcea16bProduct name220220509

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0832-1080-00EA - Each0832-108031a3c61f-ebfd-486a-84c8-209719f0438a12012-07-24

DailyMed Socrata Ingredients#

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
885219benztropine mesylate 0.5 MG Oral TabletPSNbb315aeb-1ddd-4b90-b84a-8566bb70a7532
885219benztropine mesylate 0.5 MG Oral TabletSCDbb315aeb-1ddd-4b90-b84a-8566bb70a7532

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
0832-1080-0000832108000100 TABLET in 1 BOTTLE (0832-1080-00) 100 tablet1996-12-120000-00-00NoNoCurrent