Tamsulosin Hydrochloride

Product NDC
68071-2561
11-digit product format
680712561
Labeler code
68071
Product ID
68071-2561_2dcc77bf-dfc5-3a63-e063-6394a90ad999
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Tamsulosin Hydrochloride
Dosage form
CAPSULE
Route
ORAL
Labeler
NuCare Pharmaceuticals,Inc.
Application
ANDA202433
Marketing category
ANDA
Marketing start
2013-04-30
Substance
TAMSULOSIN HYDROCHLORIDE
Active strength
.4 mg/1
Pharmacologic classes
Adrenergic alpha-Antagonists [MoA], alpha-Adrenergic Blocker [EPC]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
11SV1951MRTAMSULOSIN HYDROCHLORIDE106463-17-6TAMSULOSIN HYDROCHLORIDE

Packages

Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
68071-2561-16807125610110 CAPSULE in 1 BOTTLE (68071-2561-1) 10 capsule2021-11-02NoNoHistorical
68071-2561-36807125610330 CAPSULE in 1 BOTTLE (68071-2561-3) 30 capsule2021-11-02NoNoHistorical
68071-2561-66807125610660 CAPSULE in 1 BOTTLE (68071-2561-6) 60 capsule2021-11-02NoNoHistorical
68071-2561-96807125610990 CAPSULE in 1 BOTTLE (68071-2561-9) 90 capsule2021-11-02NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Tamsulosin HydrochlorideNuCare Pharmaceuticals,Inc.2025-02-10HUMAN PRESCRIPTION DRUG LABEL3