Doxazosin

Product NDC
51079-957
11-digit product format
510790957
Labeler code
51079
Product ID
51079-957_a59f8fda-67cb-d3bd-e053-2995a90a00e0
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
doxazosin mesylate
Dosage form
TABLET
Route
ORAL
Labeler
Mylan Institutional Inc.
Application
ANDA075509
Marketing category
ANDA
Marketing start
2001-01-01
Marketing end
2020-10-31
Substance
DOXAZOSIN MESYLATE
Active strength
1 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
51079-957-01EA - Each51079-957e42d1266-66d5-487f-a4ba-4ecbbff92f4a12012-07-24
51079-957-20EA - Each51079-9571f5ad8d5-02a9-4a19-a8d7-b3f5c001607612012-07-24