Tolterodine Tartrate

Product NDC
51079-198
11-digit product format
510790198
Labeler code
51079
Product ID
51079-198_9bca909f-8a50-70e4-e053-2995a90a3f1d
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Tolterodine Tartrate
Dosage form
CAPSULE, EXTENDED RELEASE
Route
ORAL
Labeler
Mylan Institutional Inc.
Application
ANDA201486
Marketing category
ANDA
Marketing start
2014-01-29
Marketing end
0000-00-00
Substance
TOLTERODINE TARTRATE
Active strength
4 mg/1
Pharmacologic classes
Cholinergic Muscarinic Antagonist [EPC],Cholinergic Muscarinic Antagonists [MoA]
NDC exclude flag
No
Listing certified through
2021-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
51079-198-01EA - Each51079-1982c9b6ab6-e699-49dc-ae72-0ea9b23038e012014-05-02
51079-198-03EA - Each51079-19833ced590-3827-43ee-a492-dd7492d51bb112014-04-03

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
51079-198-035107901980330 BLISTER PACK in 1 CARTON (51079-198-03) > 1 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (51079-198-01) 30 blister pack2014-01-290000-00-00NoNoCurrent