Spiriva - 0597-0075-27 - (TIOTROPIUM BROMIDE)

Alphabetical Index


Drug Information of Spiriva

Product NDC: 0597-0075
Proprietary Name: Spiriva
Non Proprietary Name: TIOTROPIUM BROMIDE
Active Ingredient(s): 18    ug/1 & nbsp;   TIOTROPIUM BROMIDE
Administration Route(s): ORAL; RESPIRATORY (INHALATION)
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Spiriva

Product NDC: 0597-0075
Labeler Name: Boehringer Ingelheim Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021395
Marketing Category: NDA
Start Marketing Date: 20051011

Package Information of Spiriva

Package NDC: 0597-0075-27
Package Description: 1 BLISTER PACK in 1 CARTON (0597-0075-27) > 10 CAPSULE in 1 BLISTER PACK

NDC Information of Spiriva

NDC Code 0597-0075-27
Proprietary Name Spiriva
Package Description 1 BLISTER PACK in 1 CARTON (0597-0075-27) > 10 CAPSULE in 1 BLISTER PACK
Product NDC 0597-0075
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name TIOTROPIUM BROMIDE
Dosage Form Name CAPSULE
Route Name ORAL; RESPIRATORY (INHALATION)
Start Marketing Date 20051011
Marketing Category Name NDA
Labeler Name Boehringer Ingelheim Pharmaceuticals Inc.
Substance Name TIOTROPIUM BROMIDE MONOHYDRATE
Strength Number 18
Strength Unit ug/1
Pharmaceutical Classes Anticholinergic [EPC],Cholinergic Antagonists [MoA]

Complete Information of Spiriva


General Information