Guanfacine Hydrochloride

Product NDC
42291-311
11-digit product format
422910311
Labeler code
42291
Product ID
42291-311_78d8920c-2afc-386a-e053-2991aa0a2d73
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Guanfacine Hydrochloride
Dosage form
TABLET
Route
ORAL
Labeler
AvKARE, Inc.
Application
ANDA075109
Marketing category
ANDA
Marketing start
2011-03-03
Marketing end
0000-00-00
Substance
GUANFACINE HYDROCHLORIDE
Active strength
2 mg/1
Pharmacologic classes
Central alpha-2 Adrenergic Agonist [EPC],Adrenergic alpha2-Agonists [MoA]
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
42291-311-90EA - Each42291-31114641403-6408-4422-a96e-367d52d4b1d612013-02-13