Doxazosin

Product NDC
55700-648
11-digit product format
557000648
Labeler code
55700
Product ID
55700-648_6477400e-20a2-4eba-9188-21cd41ba036e
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Doxazosin Mesylate
Dosage form
TABLET
Route
ORAL
Labeler
Lake Erie Medical DBA Quality Care Products LLC
Application
ANDA075536
Marketing category
ANDA
Marketing start
2018-07-06
Marketing end
0000-00-00
Substance
DOXAZOSIN MESYLATE
Active strength
2 mg/1
Pharmacologic classes
Adrenergic alpha-Antagonists [MoA],alpha-Adrenergic Blocker [EPC]
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
86P6PQK0MUDOXAZOSIN MESYLATE77883-43-3DOXAZOSIN MESYLATE