Doxazosin

Product NDC
68645-465
11-digit product format
686450465
Labeler code
68645
Product ID
68645-465_814ec517-9a88-4263-9c8b-c51188503fdb
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Doxazosin
Dosage form
TABLET
Route
ORAL
Labeler
Legacy Pharmaceutical Packaging, LLC
Application
ANDA075580
Marketing category
ANDA
Marketing start
2011-07-14
Marketing end
2020-06-30
Substance
DOXAZOSIN MESYLATE
Active strength
8 mg/1
Pharmacologic classes
Adrenergic alpha-Antagonists [MoA],alpha-Adrenergic Blocker [EPC]
NDC exclude flag
No
Listing certified through
0000-00-00
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
68645-465-54EA - Each68645-46551f2c913-99ca-4775-8569-ab879664f1cf12017-03-06
68645-465-70EA - Each68645-465e5e4b0c5-a173-41c3-80b2-d5fcaab206f912013-09-04