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Tolterodine Tartrate - 60505-3528-7 - (Tolterodine Tartrate)

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Drug Information of Tolterodine Tartrate

Product NDC: 60505-3528
Proprietary Name: Tolterodine Tartrate
Non Proprietary Name: Tolterodine Tartrate
Active Ingredient(s): 2    mg/1 & nbsp;   Tolterodine Tartrate
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Tolterodine Tartrate

Product NDC: 60505-3528
Labeler Name: Apotex Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA200164
Marketing Category: ANDA
Start Marketing Date: 20120925

Package Information of Tolterodine Tartrate

Package NDC: 60505-3528-7
Package Description: 14 BLISTER PACK in 1 CARTON (60505-3528-7) > 10 TABLET, FILM COATED in 1 BLISTER PACK

NDC Information of Tolterodine Tartrate

NDC Code 60505-3528-7
Proprietary Name Tolterodine Tartrate
Package Description 14 BLISTER PACK in 1 CARTON (60505-3528-7) > 10 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC 60505-3528
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Tolterodine Tartrate
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20120925
Marketing Category Name ANDA
Labeler Name Apotex Corp.
Substance Name TOLTERODINE TARTRATE
Strength Number 2
Strength Unit mg/1
Pharmaceutical Classes Cholinergic Muscarinic Antagonist [EPC],Cholinergic Muscarinic Antagonists [MoA]

Complete Information of Tolterodine Tartrate


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