Clonidine Hydrochloride

Product NDC
55289-970
11-digit product format
552890970
Labeler code
55289
Product ID
55289-970_7c4889dd-2a50-f1ec-e053-2991aa0a0e0c
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
clonidine hydrochloride
Dosage form
TABLET
Route
ORAL
Labeler
PD-Rx Pharmaceuticals, Inc.
Application
ANDA070317
Marketing category
ANDA
Marketing start
1987-06-09
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
55289-970-30EA - Each55289-970e98daa16-b8d7-4f6e-9967-165b34dd4cea12012-07-24