Benztropine Mesylate

Product NDC
14789-300
11-digit product format
147890300
Labeler code
14789
Product ID
14789-300_bbacbb05-2e18-4cf9-b239-6addb60b7533
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
BENZTROPINE MESYLATE
Dosage form
INJECTION
Route
PARENTERAL
Labeler
Nexus Pharmaceuticals Inc
Application
ANDA090233
Marketing category
ANDA
Marketing start
2009-07-29
Marketing end
0000-00-00
Substance
BENZTROPINE MESYLATE
Active strength
1 mg/mL
Pharmacologic classes
Anticholinergic [EPC],Antihistamine [EPC],Cholinergic Antagonists [MoA],Histamine Receptor Antagonists [MoA]
NDC exclude flag
E
Listing certified through
2017-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
14789-300-022023-09-26C16284748780-1956f9ecf-d35c-621f-e053-dbdaa90a74adbbacbb05-2e18-4cf9-b239-6addb60b7533
14789-300-022019-10-21C16284748780-1956f9ecf-d35c-621f-e053-dbdaa90a74adbbacbb05-2e18-4cf9-b239-6addb60b7533

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
14789-300-02ML - Milliliter14789-3003b626039-73a7-444c-8344-6fd77adf6aff12012-07-24