Prazosin Hydrochloride

Product NDC
63629-6873
11-digit product format
636296873
Labeler code
63629
Product ID
63629-6873_f4862d3e-f96f-422e-9da6-34c4fd4e0826
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Prazosin Hydrochloride
Dosage form
CAPSULE
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA071745
Marketing category
ANDA
Marketing start
2007-02-22
Marketing end
0000-00-00
Substance
PRAZOSIN HYDROCHLORIDE
Active strength
2 mg/1
Pharmacologic classes
alpha-Adrenergic Blocker [EPC],Adrenergic alpha-Antagonists [MoA]
NDC exclude flag
No
Listing certified through
2021-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
63629-6873-16362968730130 CAPSULE in 1 BOTTLE (63629-6873-1) 30 capsule2015-12-240000-00-00NoNoCurrent
63629-6873-26362968730228 CAPSULE in 1 BOTTLE (63629-6873-2) 28 capsule2015-12-240000-00-00NoNoCurrent
63629-6873-36362968730360 CAPSULE in 1 BOTTLE (63629-6873-3) 60 capsule2015-12-240000-00-00NoNoCurrent
63629-6873-46362968730490 CAPSULE in 1 BOTTLE (63629-6873-4) 90 capsule2015-12-240000-00-00NoNoCurrent
63629-6873-56362968730518 CAPSULE in 1 BOTTLE (63629-6873-5) 18 capsule2015-12-240000-00-00NoNoCurrent