Tamsulosin Hydrochloride

Product NDC
68788-7780
11-digit product format
687887780
Labeler code
68788
Product ID
68788-7780_f02ca352-3171-4a33-9212-4a56e9653407
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Tamsulosin Hydrochloride
Dosage form
CAPSULE
Route
ORAL
Labeler
Preferred Pharmaceuticals, Inc.
Application
ANDA204645
Marketing category
ANDA
Marketing start
2020-09-01
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

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
68788-7780-168788778001100 CAPSULE in 1 BOTTLE (68788-7780-1) 100 capsule2020-09-010000-00-00NoNoCurrent
68788-7780-26878877800220 CAPSULE in 1 BOTTLE (68788-7780-2) 20 capsule2020-09-010000-00-00NoNoCurrent
68788-7780-36878877800330 CAPSULE in 1 BOTTLE (68788-7780-3) 30 capsule2020-09-010000-00-00NoNoCurrent
68788-7780-66878877800660 CAPSULE in 1 BOTTLE (68788-7780-6) 60 capsule2020-09-010000-00-00NoNoCurrent
68788-7780-868788778008120 CAPSULE in 1 BOTTLE (68788-7780-8) 120 capsule2020-09-010000-00-00NoNoCurrent
68788-7780-96878877800990 CAPSULE in 1 BOTTLE (68788-7780-9) 90 capsule2020-09-010000-00-00NoNoCurrent