Clonidine Hydrochloride

Product NDC
0378-0199
11-digit product format
003780199
Labeler code
0378
Product ID
0378-0199_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
0378-0199-01EA - Each0378-019975568331-4d12-46e3-8fe1-565ca9f2247812012-07-24