Clonidine Hydrochloride

Product NDC
50090-2600
11-digit product format
500902600
Labeler code
50090
Product ID
50090-2600_da1aee4d-c5fc-45bd-a07a-4ce79ccbbb3e
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Clonidine Hydrochloride
Dosage form
TABLET
Route
ORAL
Labeler
A-S Medication Solutions
Application
ANDA202297
Marketing category
ANDA
Marketing start
2013-06-17
Marketing end
0000-00-00
Substance
CLONIDINE HYDROCHLORIDE
Active strength
0 mg/1
Pharmacologic classes
Adrenergic alpha2-Agonists [MoA],Central alpha-2 Adrenergic Agonist [EPC]
NDC exclude flag
No
Listing certified through
2019-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
50090-2600-0EA - Each50090-26004d058e1d-590c-4d26-b5e2-8122a4f7af8112019-04-11
50090-2600-5EA - Each50090-26009e680a42-9568-4c1e-bd01-23f63ca3d1c612019-04-11
50090-2600-6EA - Each50090-26004445898d-7eef-48be-a7b1-fc26fada8f3012019-04-11