Clonidine Hydrochloride

Product NDC
0378-0152
11-digit product format
003780152
Labeler code
0378
Product ID
0378-0152_c16087c0-cf3a-46c3-8151-81895c298888
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
clonidine hydrochloride
Dosage form
TABLET
Route
ORAL
Labeler
Mylan Pharmaceuticals Inc.
Application
ANDA070317
Marketing category
ANDA
Marketing start
1987-06-09
Marketing end
2020-09-30
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
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
0378-0152-01EA - Each0378-0152420f5c75-faf6-4997-8257-be39d863e67c12012-07-24
0378-0152-10EA - Each0378-01527f09fd29-e43d-4e40-ad4d-32b9bd72914212012-07-24