Clonidine Hydrochloride

Product NDC
51079-301
11-digit product format
510790301
Labeler code
51079
Product ID
51079-301_9a250335-e14c-c9ad-e053-2a95a90a08c8
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
clonidine hydrochloride
Dosage form
TABLET
Route
ORAL
Labeler
Mylan Institutional Inc.
Application
ANDA070317
Marketing category
ANDA
Marketing start
1995-06-12
Marketing end
2020-02-29
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
51079-301-01EA - Each51079-30182ec5aec-3c8a-4c58-a419-7e980a5862d712012-07-24
51079-301-20EA - Each51079-301d5ab2b8e-d2f3-456b-b32e-15cf6a71294312012-07-24
51079-301-63EA - Each51079-3014b22c132-9855-45e5-8089-ef687fe2484112012-07-24
51079-301-66EA - Each51079-3018db3782c-b88c-4f4d-a36c-952d5b24768612013-04-01