Tamsulosin Hydrochloride

Product NDC
68071-2859
11-digit product format
680712859
Labeler code
68071
Product ID
68071-2859_ebf29976-4798-da8b-e053-2995a90a5acf
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Tamsulosin Hydrochloride
Dosage form
CAPSULE
Route
ORAL
Labeler
NuCare Pharmaceuticals,Inc.
Application
ANDA090931
Marketing category
ANDA
Marketing start
2010-07-15
Marketing end
0000-00-00
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
2023-12-31
Current FDA listing
Historical FDA.report record

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
ee39297f-c54b-4394-13fa-e0de7b5b9070Product name420250305
ae349df8-97ce-a639-ed32-50a4cb01b1bdProduct name420200313

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
68071-2859-1Tamsulosin Hydrochloride100 in 1 BOTTLECAPSULE1001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
68071-2859TAMSULOSIN HYDROCHLORIDE CAPSULE [NUCARE PHARMACEUTICALS,INC.]1Legacy NDC, 1 package rows20221029_ebf2996d-7094-d5a3-e053-2995a90a3af0.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
863669tamsulosin HCl 0.4 MG Oral CapsulePSNebf2996d-7094-d5a3-e053-2995a90a3af01
863669tamsulosin hydrochloride 0.4 MG Oral CapsuleSCDebf2996d-7094-d5a3-e053-2995a90a3af01
863669tamsulosin HCl 0.4 MG Modified Release Oral CapsuleSYebf2996d-7094-d5a3-e053-2995a90a3af01

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
68071-2859-168071285901100 CAPSULE in 1 BOTTLE (68071-2859-1) 100 capsule2022-10-260000-00-00NoNoCurrent