Tamsulosin Hydrochloride

Product NDC
0378-2500
11-digit product format
003782500
Labeler code
0378
Product ID
0378-2500_d71e940c-17b7-46a0-b95d-e484594aa4b7
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
tamsulosin hydrochloride
Dosage form
CAPSULE
Route
ORAL
Labeler
Mylan Pharmaceuticals Inc.
Application
ANDA090408
Marketing category
ANDA
Marketing start
2010-04-27
Marketing end
2019-11-30
Substance
TAMSULOSIN HYDROCHLORIDE
Active strength
0 mg/1
Pharmacologic classes
Adrenergic alpha-Antagonists [MoA],alpha-Adrenergic Blocker [EPC]
NDC exclude flag
No
Listing certified through
0000-00-00
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0378-2500-10EA - Each0378-25009cebc1b8-44ff-4047-bdd8-485574b7f9be12012-07-24
0378-2500-77EA - Each0378-25006a8ad7d1-b236-4575-ac13-bdb9fc21b54a12012-07-24
0378-2500-93EA - Each0378-2500748a4959-ae1c-461c-868a-c464ea2ab4f712012-07-24