Prazosin Hydrochloride

Product NDC
68788-8067
11-digit product format
687888067
Labeler code
68788
Product ID
68788-8067_39a20e17-c51a-426b-831f-d911a578891c
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
prazosin hydrochloride
Dosage form
CAPSULE
Route
ORAL
Labeler
Preferred Pharmaceuticals Inc.
Application
ANDA072575
Marketing category
ANDA
Marketing start
2021-08-16
Marketing end
0000-00-00
Substance
PRAZOSIN HYDROCHLORIDE
Active strength
5 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
68788-8067-168788806701100 CAPSULE in 1 BOTTLE, PLASTIC (68788-8067-1) 100 capsule2021-08-160000-00-00NoNoCurrent
68788-8067-36878880670330 CAPSULE in 1 BOTTLE, PLASTIC (68788-8067-3) 30 capsule2021-08-160000-00-00NoNoCurrent
68788-8067-66878880670660 CAPSULE in 1 BOTTLE, PLASTIC (68788-8067-6) 60 capsule2021-08-160000-00-00NoNoCurrent
68788-8067-96878880670990 CAPSULE in 1 BOTTLE, PLASTIC (68788-8067-9) 90 capsule2021-08-160000-00-00NoNoCurrent